Canonical Allele Identifier: CA48454290
Gene: FAM161A HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
XR_939724.1:n.4220-18980C>T
XR_001739092.1:n.493C>T
Search 100 bp 5'
Search 100 bp 3'