Canonical Allele Identifier: CA54648391
Gene:

Linked Data

dbSNP Id: rs199624562

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332295G>C , CM000664.2:g.120332295G>C GRCh38
NC_000002.11:g.121089871G>C , CM000664.1:g.121089871G>C GRCh37
NC_000002.10:g.120806341G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3489G>C XP_011510609.1:n.141+3489G>C