Canonical Allele Identifier: CA198781184

Gene:

Linked Data

• dbSNP Id: rs930561069
• MyVariant Identifiers: chr9:g.120559140A>T (hg19) ; chr9:g.117796862A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.117796862A>T , CM000671.2:g.117796862A>T	GRCh38
NC_000009.11:g.120559140A>T , CM000671.1:g.120559140A>T	GRCh37
NC_000009.10:g.119598961A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646089.2:c.94-51203A>T	ENSP00000496197.1:n.94-51203A>T
ENST00000697624.1:n.201-51203A>T
ENST00000697636.1:c.94-51203A>T	ENSP00000513366.1:n.94-51203A>T
ENST00000697637.1:c.94-51203A>T	ENSP00000513367.1:n.94-51203A>T
ENST00000697664.1:c.*86+29612A>T	ENSP00000513389.1:n.*86+29612A>T
ENST00000697665.1:c.94-51203A>T	ENSP00000513390.1:n.94-51203A>T
ENST00000697666.1:c.141-51203A>T	ENSP00000513391.1:n.141-51203A>T
ENST00000642985.1:c.261-51203A>T	ENSP00000493686.1:n.261-51203A>T
ENST00000646089.1:c.94-51203A>T	ENSP00000496197.1:n.94-51203A>T
ENST00000665764.1:c.94-51203A>T	ENSP00000499745.1:n.94-51203A>T
XR_930289.1:n.1628-6119A>T
XR_001746915.1:n.2244-6119A>T