Canonical Allele Identifier: CA290433269
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs896219708
gnomAD v3: 17-39664901-C-T
gnomAD v4: 17-39664901-C-T
MyVariant Identifiers: chr17:g.37821154C>T (hg19) chr17:g.39664901C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664901C>T , CM000679.2:g.39664901C>T GRCh38
NC_000017.10:g.37821154C>T , CM000679.1:g.37821154C>T GRCh37
NC_000017.9:g.35074680C>T NCBI36
NG_008892.1:g.4556C>T , LRG_210:g.4556C>T
NG_042278.1:g.1921C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-459C>T ENSP00000312624.2:n.-459C>T
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