Canonical Allele Identifier: CA1035662720
Gene:

Linked Data

dbSNP Id: rs1690914797

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120332209T>C , CM000664.2:g.120332209T>C GRCh38
NC_000002.11:g.121089785T>C , CM000664.1:g.121089785T>C GRCh37
NC_000002.10:g.120806255T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512307.1:c.141+3403T>C XP_011510609.1:n.141+3403T>C