Canonical Allele Identifier: CA64382894
Gene:

Linked Data

dbSNP Id: rs752255485
MyVariant Identifiers: chr2:g.200897909A>G (hg19) chr2:g.200033186A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033186A>G , CM000664.2:g.200033186A>G GRCh38
NC_000002.11:g.200897909A>G , CM000664.1:g.200897909A>G GRCh37
NC_000002.10:g.200606154A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22290T>C
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