Canonical Allele Identifier: CA1827951922

Gene: SMARCA2

Linked Data

• dbSNP Id: rs184207684

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.2116236C>T , CM000671.2:g.2116236C>T	GRCh38
NC_000009.11:g.2116236C>T , CM000671.1:g.2116236C>T	GRCh37
NC_000009.10:g.2106236C>T	NCBI36
NG_032162.1:g.105895C>T
NG_032162.2:g.140947C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704350.1:c.3324+187C>T	ENSP00000515861.1:n.3324+187C>T
ENST00000704352.1:c.1174-45450C>T	ENSP00000515863.1:n.1174-45450C>T
ENST00000704353.1:c.1174-45450C>T	ENSP00000515864.1:n.1174-45450C>T
ENST00000704354.1:c.3668+187C>T
ENST00000704355.1:c.2048+187C>T
ENST00000349721.8:c.3684+187C>T MANE Select	ENSP00000265773.5:n.3684+187C>T
ENST00000357248.8:c.3684+187C>T	ENSP00000349788.2:n.3684+187C>T
ENST00000635739.1:n.2352+187C>T
ENST00000636157.1:n.1291+187C>T
ENST00000638139.1:n.718+187C>T
ENST00000349721.7:c.3684+187C>T	ENSP00000265773.5:n.3684+187C>T
ENST00000357248.7:c.3684+187C>T	ENSP00000349788.2:n.3684+187C>T
ENST00000382194.6:c.3684+187C>T	ENSP00000371629.1:n.3684+187C>T
ENST00000382203.5:c.3684+187C>T	ENSP00000371638.1:n.3684+187C>T
ENST00000450198.6:c.3510+187C>T	ENSP00000392081.2:n.3510+187C>T
ENST00000634760.1:c.3684+187C>T	ENSP00000489256.1:n.3684+187C>T
ENST00000634772.1:c.62-3222C>T
ENST00000634925.1:n.1175+187C>T
NM_001289396.1:c.3684+187C>T	NP_001276325.1:n.3684+187C>T
NM_001289397.1:c.3510+187C>T	NP_001276326.1:n.3510+187C>T
NM_003070.4:c.3684+187C>T	NP_003061.3:n.3684+187C>T
NM_139045.3:c.3684+187C>T	NP_620614.2:n.3684+187C>T
NM_003070.5:c.3684+187C>T MANE Select	NP_003061.3:n.3684+187C>T
NM_001289397.2:c.3510+187C>T	NP_001276326.1:n.3510+187C>T
NM_139045.4:c.3684+187C>T	NP_620614.2:n.3684+187C>T