Canonical Allele Identifier: CA11054067
Gene:

Linked Data

dbSNP Id: rs10206020
gnomAD v2: 2-1557927-T-C
gnomAD v3: 2-1554155-T-C
gnomAD v4: 2-1554155-T-C
MyVariant Identifiers: chr2:g.1557927T>C (hg19) chr2:g.1554155T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.1554155T>C , CM000664.2:g.1554155T>C GRCh38
NC_000002.11:g.1557927T>C , CM000664.1:g.1557927T>C GRCh37
NC_000002.10:g.1536934T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011510447.1:c.-1018T>C XP_011508749.1:n.-1018T>C
XM_011510448.1:c.-1018T>C XP_011508750.1:n.-1018T>C
XR_922720.1:n.85+2343A>G
XM_017005455.1:c.-1018T>C XP_016860944.1:n.-1018T>C
NR_168373.1:n.746-15T>C
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