Canonical Allele Identifier: CA499889134
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs2145073640
gnomAD v3: 17-39665848-C-T
gnomAD v4: 17-39665848-C-T
MyVariant Identifiers: chr17:g.37822101C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665848C>T , CM000679.2:g.39665848C>T GRCh38
NC_000017.10:g.37822101C>T , CM000679.1:g.37822101C>T GRCh37
NC_000017.9:g.35075627C>T NCBI36
NG_008892.1:g.5503C>T , LRG_210:g.5503C>T
NG_042278.1:g.2868C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.243C>T MANE Select ENSP00000312624.2:p.Tyr81=
ENST00000309889.2:c.243C>T ENSP00000312624.2:p.Tyr81=
ENST00000578283.1:c.175-4C>T ENSP00000462787.1:n.175-4C>T
NM_003673.3:c.243C>T , LRG_210t1:c.243C>T NP_003664.1:p.Tyr81=
NM_003673.4:c.243C>T MANE Select NP_003664.1:p.Tyr81=
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