Canonical Allele Identifier: CA1284436090
Gene:

Linked Data

dbSNP Id: rs899506182

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379268C>G , CM000664.2:g.122379268C>G GRCh38
NC_000002.11:g.123136844C>G , CM000664.1:g.123136844C>G GRCh37
NC_000002.10:g.122853314C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-13695C>G
XR_001739684.1:n.556-13695C>G