Canonical Allele Identifier: CA983628819
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2057242961
gnomAD v3: 17-39664922-G-C
gnomAD v4: 17-39664922-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664922G>C , CM000679.2:g.39664922G>C GRCh38
NC_000017.10:g.37821175G>C , CM000679.1:g.37821175G>C GRCh37
NC_000017.9:g.35074701G>C NCBI36
NG_008892.1:g.4577G>C , LRG_210:g.4577G>C
NG_042278.1:g.1942G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-438G>C ENSP00000312624.2:n.-438G>C
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