Canonical Allele Identifier: CA422484492
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769746C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800616C>G , CM000663.2:g.192800616C>G GRCh38
NC_000001.10:g.192769746C>G , CM000663.1:g.192769746C>G GRCh37
NC_000001.9:g.191036369C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.46C>G