Canonical Allele Identifier: CA237744454

Gene: STAT6

Linked Data

• dbSNP Id: rs567048191
• gnomAD v3: 12-57095945-A-G
• gnomAD v4: 12-57095945-A-G
• MyVariant Identifiers: chr12:g.57489728A>G (hg19) ; chr12:g.57095945A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.57095945A>G , CM000674.2:g.57095945A>G	GRCh38
NC_000012.11:g.57489728A>G , CM000674.1:g.57489728A>G	GRCh37
NC_000012.10:g.55775995A>G	NCBI36
NG_021272.1:g.20469T>C
NG_021272.2:g.41195T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300134.8:c.*627T>C MANE Select	ENSP00000300134.3:n.*627T>C
ENST00000553533.2:c.*627T>C	ENSP00000451546.2:n.*627T>C
ENST00000554764.6:c.*2915T>C	ENSP00000451909.1:n.*2915T>C
ENST00000651176.1:c.*961T>C	ENSP00000498693.1:n.*961T>C
ENST00000300134.7:c.*627T>C	ENSP00000300134.3:n.*627T>C
ENST00000555222.5:n.2144T>C
NM_001178078.1:c.*627T>C	NP_001171549.1:n.*627T>C
NM_001178079.1:c.*627T>C	NP_001171550.1:n.*627T>C
NM_001178080.1:c.*627T>C	NP_001171551.1:n.*627T>C
NM_001178081.1:c.*627T>C	NP_001171552.1:n.*627T>C
NM_003153.4:c.*627T>C	NP_003144.3:n.*627T>C
NR_033659.1:n.3338T>C
XM_006719574.1:c.*627T>C	XP_006719637.1:n.*627T>C
XM_006719575.1:c.*627T>C	XP_006719638.1:n.*627T>C
XM_011538703.1:c.*627T>C	XP_011537005.1:n.*627T>C
XM_011538704.1:c.*627T>C	XP_011537006.1:n.*627T>C
XM_011538705.1:c.*627T>C	XP_011537007.1:n.*627T>C
XM_011538706.1:c.*627T>C	XP_011537008.1:n.*627T>C
XM_011538707.1:c.*627T>C	XP_011537009.1:n.*627T>C
XM_011538708.1:c.*627T>C	XP_011537010.1:n.*627T>C
XM_011538709.1:c.*627T>C	XP_011537011.1:n.*627T>C
XM_011538703.3:c.*627T>C	XP_011537005.1:n.*627T>C
XM_011538704.3:c.*627T>C	XP_011537006.1:n.*627T>C
XM_011538705.3:c.*627T>C	XP_011537007.1:n.*627T>C
XM_011538707.3:c.*627T>C	XP_011537009.1:n.*627T>C
XM_011538708.3:c.*627T>C	XP_011537010.1:n.*627T>C
NM_003153.5:c.*627T>C MANE Select	NP_003144.3:n.*627T>C
NM_001178078.2:c.*627T>C	NP_001171549.1:n.*627T>C
NM_001178079.2:c.*627T>C	NP_001171550.1:n.*627T>C
NM_001178080.2:c.*627T>C	NP_001171551.1:n.*627T>C
NM_001178081.2:c.*627T>C	NP_001171552.1:n.*627T>C
NR_033659.2:n.3287T>C