Canonical Allele Identifier: CA290433334
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs986202883
gnomAD v2: 17-37821230-G-T
gnomAD v3: 17-39664977-G-T
gnomAD v4: 17-39664977-G-T
MyVariant Identifiers: chr17:g.37821230G>T (hg19) chr17:g.39664977G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664977G>T , CM000679.2:g.39664977G>T GRCh38
NC_000017.10:g.37821230G>T , CM000679.1:g.37821230G>T GRCh37
NC_000017.9:g.35074756G>T NCBI36
NG_008892.1:g.4632G>T , LRG_210:g.4632G>T
NG_042278.1:g.1997G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-383G>T ENSP00000312624.2:n.-383G>T
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