Canonical Allele Identifier: CA2259200351
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057244442
gnomAD v4: 17-39665111-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665111G>C , CM000679.2:g.39665111G>C GRCh38
NC_000017.10:g.37821364G>C , CM000679.1:g.37821364G>C GRCh37
NC_000017.9:g.35074890G>C NCBI36
NG_008892.1:g.4766G>C , LRG_210:g.4766G>C
NG_042278.1:g.2131G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-249G>C ENSP00000312624.2:n.-249G>C
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