Canonical Allele Identifier: CA756180388
Gene:

Linked Data

dbSNP Id: rs1164568750

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379247G>T , CM000664.2:g.122379247G>T GRCh38
NC_000002.11:g.123136823G>T , CM000664.1:g.123136823G>T GRCh37
NC_000002.10:g.122853293G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-13716G>T
XR_001739684.1:n.556-13716G>T