Canonical Allele Identifier: CA859265936

Gene:

Linked Data

• dbSNP Id: rs1273917179
• gnomAD v3: 9-117796619-A-G
• gnomAD v4: 9-117796619-A-G
• MyVariant Identifiers: chr9:g.120558897A>G (hg19) ; chr9:g.117796619A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117796619A>G , CM000671.2:g.117796619A>G	GRCh38
NC_000009.11:g.120558897A>G , CM000671.1:g.120558897A>G	GRCh37
NC_000009.10:g.119598718A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.94-51446A>G	ENSP00000496197.1:n.94-51446A>G
ENST00000697624.1:n.201-51446A>G
ENST00000697636.1:c.94-51446A>G	ENSP00000513366.1:n.94-51446A>G
ENST00000697637.1:c.94-51446A>G	ENSP00000513367.1:n.94-51446A>G
ENST00000697664.1:c.*86+29369A>G	ENSP00000513389.1:n.*86+29369A>G
ENST00000697665.1:c.94-51446A>G	ENSP00000513390.1:n.94-51446A>G
ENST00000697666.1:c.141-51446A>G	ENSP00000513391.1:n.141-51446A>G
ENST00000642985.1:c.261-51446A>G	ENSP00000493686.1:n.261-51446A>G
ENST00000646089.1:c.94-51446A>G	ENSP00000496197.1:n.94-51446A>G
ENST00000665764.1:c.94-51446A>G	ENSP00000499745.1:n.94-51446A>G
XR_930289.1:n.1628-6362A>G
XR_001746915.1:n.2244-6362A>G