Canonical Allele Identifier: CA63825742
Gene:

Linked Data

dbSNP Id: rs539335082
gnomAD v2: 2-204800870-C-T
gnomAD v3: 2-203936147-C-T
gnomAD v4: 2-203936147-C-T
MyVariant Identifiers: chr2:g.204800870C>T (hg19) chr2:g.203936147C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.203936147C>T , CM000664.2:g.203936147C>T GRCh38
NC_000002.11:g.204800870C>T , CM000664.1:g.204800870C>T GRCh37
NC_000002.10:g.204509115C>T NCBI36
NG_011586.1:g.4368C>T , LRG_65:g.4368C>T

Transcript Alleles

HGVS Amino-acid change
XR_427213.2:n.421G>A
XR_001739861.1:n.435G>A
XR_427213.3:n.435G>A
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