Canonical Allele Identifier: CA771857988
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1402269482
gnomAD v3: 17-39665579-A-G
gnomAD v4: 17-39665579-A-G
MyVariant Identifiers: chr17:g.37821832A>G (hg19) chr17:g.39665579A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39665579A>G , CM000679.2:g.39665579A>G GRCh38
NC_000017.10:g.37821832A>G , CM000679.1:g.37821832A>G GRCh37
NC_000017.9:g.35075358A>G NCBI36
NG_008892.1:g.5234A>G , LRG_210:g.5234A>G
NG_042278.1:g.2599A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.3:c.110+110A>G MANE Select ENSP00000312624.2:n.110+110A>G
ENST00000309889.2:c.110+110A>G ENSP00000312624.2:n.110+110A>G
ENST00000578283.1:c.110+110A>G ENSP00000462787.1:n.110+110A>G
NM_003673.3:c.110+110A>G , LRG_210t1:c.110+110A>G NP_003664.1:n.110+110A>G
NM_003673.4:c.110+110A>G MANE Select NP_003664.1:n.110+110A>G
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