Canonical Allele Identifier: CA422484466
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769741A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800611A>C , CM000663.2:g.192800611A>C GRCh38
NC_000001.10:g.192769741A>C , CM000663.1:g.192769741A>C GRCh37
NC_000001.9:g.191036364A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.41A>C