Canonical Allele Identifier: CA59107036
Gene:

Linked Data

dbSNP Id: rs1053506319
gnomAD v3: 2-155870157-T-C
gnomAD v4: 2-155870157-T-C
MyVariant Identifiers: chr2:g.156726669T>C (hg19) chr2:g.155870157T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870157T>C , CM000664.2:g.155870157T>C GRCh38
NC_000002.11:g.156726669T>C , CM000664.1:g.156726669T>C GRCh37
NC_000002.10:g.156434915T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-2970A>G
XR_001739749.1:n.331-29173A>G
XR_001739750.1:n.331-29173A>G
XR_001739751.1:n.331-29173A>G
XR_923501.2:n.331-2970A>G
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