Canonical Allele Identifier: CA1438624549
Gene:

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
XR_001741361.1:n.950+19174A=