Canonical Allele Identifier: CA422485102
Gene:

Linked Data

MyVariant Identifiers: chr1:g.192769884T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800754T>C , CM000663.2:g.192800754T>C GRCh38
NC_000001.10:g.192769884T>C , CM000663.1:g.192769884T>C GRCh37
NC_000001.9:g.191036507T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.184T>C
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