Canonical Allele Identifier: CA107971404
Gene:

Linked Data

dbSNP Id: rs1015926739

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148649564T>C , CM000666.2:g.148649564T>C GRCh38
NC_000004.11:g.149570716T>C , CM000666.1:g.149570716T>C GRCh37
NC_000004.10:g.149790166T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_939336.1:n.437-30696A>G
XR_001741441.1:n.1745+104980T>C
XR_939336.3:n.2921-30696A>G