Canonical Allele Identifier: CA422484940
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769839T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800709T>G , CM000663.2:g.192800709T>G GRCh38
NC_000001.10:g.192769839T>G , CM000663.1:g.192769839T>G GRCh37
NC_000001.9:g.191036462T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000429211.2:n.139T>G