Canonical Allele Identifier: CA1468682092
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.74554019T= , CM000666.2:g.74554019T= GRCh38
NC_000004.11:g.75419736T= , CM000666.1:g.75419736T= GRCh37
NC_000004.10:g.75638600T= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001741513.1:n.167-1187A=