Canonical Allele Identifier: CA2841157961
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.97269635T>C , CM000670.2:g.97269635T>C GRCh38
NC_000008.10:g.98281863T>C , CM000670.1:g.98281863T>C GRCh37
NC_000008.9:g.98351039T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_125390.1:n.471+149435A>G