Canonical Allele Identifier: CA422484951
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769843G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800713G>C , CM000663.2:g.192800713G>C GRCh38
NC_000001.10:g.192769843G>C , CM000663.1:g.192769843G>C GRCh37
NC_000001.9:g.191036466G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.143G>C