Canonical Allele Identifier: CA422484534
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769754A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800624A>C , CM000663.2:g.192800624A>C GRCh38
NC_000001.10:g.192769754A>C , CM000663.1:g.192769754A>C GRCh37
NC_000001.9:g.191036377A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.54A>C