Canonical Allele Identifier: CA366389250

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148922-G-T
• MyVariant Identifiers: chr6:g.157470056G>T (hg19) ; chr6:g.157148922G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148922G>T , CM000668.2:g.157148922G>T	GRCh38
NC_000006.11:g.157470056G>T , CM000668.1:g.157470056G>T	GRCh37
NC_000006.10:g.157511748G>T	NCBI36
NG_032093.1:g.375993G>T
NG_032093.2:g.375993G>T
NG_066624.1:g.377897G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3060G>T	ENSP00000055163.8:p.Met1020Ile
ENST00000414678.8:c.2970G>T	ENSP00000412835.3:p.Met990Ile
ENST00000637015.2:c.3060G>T	ENSP00000489729.2:p.Met1020Ile
ENST00000319584.11:c.1074G>T	ENSP00000313006.7:p.Met358Ile
ENST00000346085.10:c.3099G>T	ENSP00000344546.5:p.Met1033Ile
ENST00000350026.10:c.2811G>T	ENSP00000055163.7:p.Met937Ile
ENST00000414678.7:c.1218G>T	ENSP00000412835.2:p.Met406Ile
ENST00000452544.2:n.961G>T
ENST00000635849.1:c.381G>T	ENSP00000490948.1:p.Met127Ile
ENST00000635957.1:c.15G>T	ENSP00000490385.1:p.Met5Ile
ENST00000636426.1:n.194G>T
ENST00000636930.2:c.3060G>T MANE Select	ENSP00000490491.2:p.Met1020Ile
ENST00000637015.1:c.299G>T
ENST00000637568.1:c.103G>T
ENST00000637810.1:c.561G>T	ENSP00000489636.1:p.Met187Ile
ENST00000637904.1:c.561G>T	ENSP00000490550.1:p.Met187Ile
ENST00000647938.1:c.2850G>T	ENSP00000498155.1:p.Met950Ile
ENST00000674190.1:n.1809G>T
ENST00000319584.10:c.1077G>T	ENSP00000313006.6:p.Met359Ile
ENST00000346085.9:c.2850G>T	ENSP00000344546.4:p.Met950Ile
ENST00000350026.9:c.2811G>T	ENSP00000055163.7:p.Met937Ile
ENST00000400790.3:c.12G>T	ENSP00000383596.3:p.Met4Ile
ENST00000414678.6:c.1218G>T	ENSP00000412835.2:p.Met406Ile
ENST00000452544.1:n.907G>T
ENST00000478761.3:c.133G>T
NM_017519.2:c.2811G>T	NP_059989.2:p.Met937Ile
NM_020732.3:c.2850G>T	NP_065783.3:p.Met950Ile
XM_005267069.3:c.2811G>T	XP_005267126.2:p.Met937Ile
XM_011535984.1:c.1761G>T	XP_011534286.1:p.Met587Ile
XM_011535985.1:c.1581G>T	XP_011534287.1:p.Met527Ile
XM_011535986.1:c.1341G>T	XP_011534288.1:p.Met447Ile
XM_011535987.1:c.960G>T	XP_011534289.1:p.Met320Ile
XM_011535988.1:c.-20+15715G>T	XP_011534290.1:n.-20+15715G>T
NM_001346813.1:c.2811G>T	NP_001333742.1:p.Met937Ile
NM_001363725.1:c.561G>T	NP_001350654.1:p.Met187Ile
XM_011535984.2:c.2892G>T	XP_011534286.2:p.Met964Ile
XM_011535988.3:c.-20+15715G>T	XP_011534290.1:n.-20+15715G>T
XM_017011103.2:c.2892G>T	XP_016866592.1:p.Met964Ile
XM_017011104.1:c.2892G>T	XP_016866593.1:p.Met964Ile
XM_017011105.2:c.2892G>T	XP_016866594.1:p.Met964Ile
XM_017011106.2:c.2892G>T	XP_016866595.1:p.Met964Ile
XM_017011107.2:c.2712G>T	XP_016866596.1:p.Met904Ile
XR_002956289.1:n.2975G>T
NM_001363725.2:c.561G>T	NP_001350654.1:p.Met187Ile
NM_001371656.1:c.3099G>T	NP_001358585.1:p.Met1033Ile
NM_001374820.1:c.3099G>T	NP_001361749.1:p.Met1033Ile
NM_001374828.1:c.3060G>T MANE Select	NP_001361757.1:p.Met1020Ile
NM_017519.3:c.3060G>T	NP_059989.3:p.Met1020Ile