Canonical Allele Identifier: CA15210296
Gene:

Linked Data

dbSNP Id: rs1550404
gnomAD v2: 2-127330954-T-G
gnomAD v3: 2-126573377-T-G
gnomAD v4: 2-126573377-T-G
MyVariant Identifiers: chr2:g.127330954T>G (hg19) chr2:g.126573377T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.126573377T>G , CM000664.2:g.126573377T>G GRCh38
NC_000002.11:g.127330954T>G , CM000664.1:g.127330954T>G GRCh37
NC_000002.10:g.127047424T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011512267.1:c.403-36860A>C XP_011510569.1:n.403-36860A>C
XR_001739693.1:n.211-36860A>C
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