Canonical Allele Identifier: CA1859674697
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.82521000A>T , CM000671.2:g.82521000A>T GRCh38
NC_000009.11:g.85135915A>T , CM000671.1:g.85135915A>T GRCh37
NC_000009.10:g.84325735A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000589973.2:n.247+24142A>T
ENST00000590298.5:n.440-43029A>T
ENST00000590791.5:n.526-3519A>T
ENST00000591257.5:n.347-3519A>T
ENST00000637606.1:n.985+24142A>T
XR_001746782.1:n.241+24142A>T