Canonical Allele Identifier: CA535757857

Gene:

Linked Data

• dbSNP Id: rs1488355677
• gnomAD v2: 2-121089690-T-C
• COSMIC: COSN25402260
• MyVariant Identifiers: chr2:g.121089690T>C (hg19) ; chr2:g.120332114T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120332114T>C , CM000664.2:g.120332114T>C	GRCh38
NC_000002.11:g.121089690T>C , CM000664.1:g.121089690T>C	GRCh37
NC_000002.10:g.120806160T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XM_011512307.1:c.141+3308T>C	XP_011510609.1:n.141+3308T>C