Canonical Allele Identifier: CA59107045
Gene:

Linked Data

dbSNP Id: rs1003077446
gnomAD v2: 2-156726766-T-C
gnomAD v3: 2-155870254-T-C
gnomAD v4: 2-155870254-T-C
MyVariant Identifiers: chr2:g.156726766T>C (hg19) chr2:g.155870254T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870254T>C , CM000664.2:g.155870254T>C GRCh38
NC_000002.11:g.156726766T>C , CM000664.1:g.156726766T>C GRCh37
NC_000002.10:g.156435012T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3067A>G
XR_001739749.1:n.331-29270A>G
XR_001739750.1:n.331-29270A>G
XR_001739751.1:n.331-29270A>G
XR_923501.2:n.331-3067A>G
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