Canonical Allele Identifier: CA64382951
Gene:

Linked Data

dbSNP Id: rs757010160
gnomAD v2: 2-200898090-T-G
gnomAD v3: 2-200033367-T-G
gnomAD v4: 2-200033367-T-G
MyVariant Identifiers: chr2:g.200898090T>G (hg19) chr2:g.200033367T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.200033367T>G , CM000664.2:g.200033367T>G GRCh38
NC_000002.11:g.200898090T>G , CM000664.1:g.200898090T>G GRCh37
NC_000002.10:g.200606335T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923778.1:n.178-22471A>C
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