Canonical Allele Identifier: CA290433488
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs565479782
gnomAD v4: 17-39665221-G-C
MyVariant Identifiers: chr17:g.37821474G>C (hg19) chr17:g.39665221G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665221G>C , CM000679.2:g.39665221G>C GRCh38
NC_000017.10:g.37821474G>C , CM000679.1:g.37821474G>C GRCh37
NC_000017.9:g.35075000G>C NCBI36
NG_008892.1:g.4876G>C , LRG_210:g.4876G>C
NG_042278.1:g.2241G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-139G>C ENSP00000312624.2:n.-139G>C
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