Canonical Allele Identifier: CA535782168
Gene:

Linked Data

dbSNP Id: rs1249798343

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.122368936T>G , CM000664.2:g.122368936T>G GRCh38
NC_000002.11:g.123126512T>G , CM000664.1:g.123126512T>G GRCh37
NC_000002.10:g.122842982T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923278.1:n.556-24027T>G
XR_001739684.1:n.556-24027T>G