Canonical Allele Identifier: CA760372007
Gene:

Linked Data

dbSNP Id: rs1193327263
gnomAD v3: 2-168260432-C-G
gnomAD v4: 2-168260432-C-G
MyVariant Identifiers: chr2:g.169116942C>G (hg19) chr2:g.168260432C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168260432C>G , CM000664.2:g.168260432C>G GRCh38
NC_000002.11:g.169116942C>G , CM000664.1:g.169116942C>G GRCh37
NC_000002.10:g.168825188C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001739763.1:n.912-4664C>G
XR_001739764.1:n.318-4664C>G
XR_001739765.1:n.436-4664C>G
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