Canonical Allele Identifier: CA422484506
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769748G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800618G>A , CM000663.2:g.192800618G>A GRCh38
NC_000001.10:g.192769748G>A , CM000663.1:g.192769748G>A GRCh37
NC_000001.9:g.191036371G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.48G>A