Canonical Allele Identifier: CA422484796
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769801G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800671G>C , CM000663.2:g.192800671G>C GRCh38
NC_000001.10:g.192769801G>C , CM000663.1:g.192769801G>C GRCh37
NC_000001.9:g.191036424G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.101G>C
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