Canonical Allele Identifier: CA1255555898
Gene: FAM161A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.61764103G= , CM000664.2:g.61764103G= GRCh38
NC_000002.11:g.61991238G= , CM000664.1:g.61991238G= GRCh37
NC_000002.10:g.61844742G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939724.1:n.4220-18980C=
XR_001739092.1:n.493C=