Canonical Allele Identifier: CA107748793

Gene:

Linked Data

• dbSNP Id: rs962015606
• gnomAD v2: 4-145480959-A-G
• gnomAD v3: 4-144559807-A-G
• gnomAD v4: 4-144559807-A-G
• MyVariant Identifiers: chr4:g.145480959A>G (hg19) ; chr4:g.144559807A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.144559807A>G , CM000666.2:g.144559807A>G	GRCh38
NC_000004.11:g.145480959A>G , CM000666.1:g.145480959A>G	GRCh37
NC_000004.10:g.145700409A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649263.1:c.328-143829T>C	ENSP00000497507.1:n.328-143829T>C
XR_939272.1:n.178+2177T>C
XR_939273.1:n.178+2177T>C
XR_939272.2:n.522+2177T>C
XR_939273.2:n.522+2177T>C