Canonical Allele Identifier: CA41586285
Gene:

Linked Data

dbSNP Id: rs766518375
gnomAD v3: 2-773231-C-A
gnomAD v4: 2-773231-C-A
MyVariant Identifiers: chr2:g.773231C>A (hg19) chr2:g.773231C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.773231C>A , CM000664.2:g.773231C>A GRCh38
NC_000002.11:g.773231C>A , CM000664.1:g.773231C>A GRCh37
NC_000002.10:g.763231C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011510439.1:c.-24-3605C>A XP_011508741.1:n.-24-3605C>A
XM_011510440.1:c.-24-3605C>A XP_011508742.1:n.-24-3605C>A
XM_011510441.1:c.-24-3605C>A XP_011508743.1:n.-24-3605C>A
XM_011510442.1:c.-24-3605C>A XP_011508744.1:n.-24-3605C>A
XM_011510443.1:c.-24-3605C>A XP_011508745.1:n.-24-3605C>A
XR_922708.1:n.4001-3605C>A
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