Canonical Allele Identifier: CA2705173359
Gene:

Linked Data

dbSNP Id: rs2108921596

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.12578045T>C , CM000666.2:g.12578045T>C GRCh38
NC_000004.11:g.12579669T>C , CM000666.1:g.12579669T>C GRCh37
NC_000004.10:g.12188767T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_925406.1:n.106+31297A>G
XR_001741374.1:n.254+44610A>G
XR_925406.3:n.140+31297A>G