Canonical Allele Identifier: CA54648352
Gene:

Linked Data

dbSNP Id: rs181625475

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332163C>T , CM000664.2:g.120332163C>T GRCh38
NC_000002.11:g.121089739C>T , CM000664.1:g.121089739C>T GRCh37
NC_000002.10:g.120806209C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3357C>T XP_011510609.1:n.141+3357C>T