Canonical Allele Identifier: CA422484908
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769829C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800699C>A , CM000663.2:g.192800699C>A GRCh38
NC_000001.10:g.192769829C>A , CM000663.1:g.192769829C>A GRCh37
NC_000001.9:g.191036452C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.129C>A