Canonical Allele Identifier: CA11216177
Gene:

Linked Data

dbSNP Id: rs4663302
gnomAD v2: 2-239203761-T-C
gnomAD v3: 2-238295120-T-C
gnomAD v4: 2-238295120-T-C
MyVariant Identifiers: chr2:g.239203761T>C (hg19) chr2:g.238295120T>C (hg38)
Allelic Epigenome: Alellic Epigenome (raw data)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.238295120T>C , CM000664.2:g.238295120T>C GRCh38
NC_000002.11:g.239203761T>C , CM000664.1:g.239203761T>C GRCh37
NC_000002.10:g.238868500T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_002959458.1:n.103-3257T>C
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