Canonical Allele Identifier: CA1438624550
Gene:

Linked Data

dbSNP Id: rs1577111526

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.11502020A>C , CM000666.2:g.11502020A>C GRCh38
NC_000004.11:g.11503644A>C , CM000666.1:g.11503644A>C GRCh37
NC_000004.10:g.11112742A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741361.1:n.950+19174A>C