Canonical Allele Identifier: CA760016613
Gene:

Linked Data

dbSNP Id: rs928048499
MyVariant Identifiers: chr2:g.16639416A>G (hg19) chr2:g.16458148A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.16458148A>G , CM000664.2:g.16458148A>G GRCh38
NC_000002.11:g.16639416A>G , CM000664.1:g.16639416A>G GRCh37
NC_000002.10:g.16502897A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_939752.1:n.396-3054T>C
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