Canonical Allele Identifier: CA1283487429
Gene:

Linked Data

dbSNP Id: rs1690909910

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.120331865C>A , CM000664.2:g.120331865C>A GRCh38
NC_000002.11:g.121089441C>A , CM000664.1:g.121089441C>A GRCh37
NC_000002.10:g.120805911C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512307.1:c.141+3059C>A XP_011510609.1:n.141+3059C>A