Canonical Allele Identifier: CA54648300

Gene:

Linked Data

• dbSNP Id: rs948198854
• gnomAD v2: 2-121089581-G-C
• gnomAD v3: 2-120332005-G-C
• gnomAD v4: 2-120332005-G-C
• MyVariant Identifiers: chr2:g.121089581G>C (hg19) ; chr2:g.120332005G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120332005G>C , CM000664.2:g.120332005G>C	GRCh38
NC_000002.11:g.121089581G>C , CM000664.1:g.121089581G>C	GRCh37
NC_000002.10:g.120806051G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011512307.1:c.141+3199G>C	XP_011510609.1:n.141+3199G>C