Canonical Allele Identifier: CA1035797158
Gene:

Linked Data

dbSNP Id: rs1679098290

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122379282A>G , CM000664.2:g.122379282A>G GRCh38
NC_000002.11:g.123136858A>G , CM000664.1:g.123136858A>G GRCh37
NC_000002.10:g.122853328A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923278.1:n.556-13681A>G
XR_001739684.1:n.556-13681A>G