Canonical Allele Identifier: CA1502632269
Community Standard Title: NC_000004.12:g.148713873C=
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.148713873C= , CM000666.2:g.148713873C= GRCh38
NC_000004.11:g.149635025C= , CM000666.1:g.149635025C= GRCh37
NC_000004.10:g.149854475C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001741441.1:n.1746-152884C=