Canonical Allele Identifier: CA625938588
Gene: TCAP HGNC NCBI

Linked Data

dbSNP Id: rs1315197293
gnomAD v2: 17-37821149-ACT-A
gnomAD v3: 17-39664896-ACT-A
gnomAD v4: 17-39664896-ACT-A
MyVariant Identifiers: chr17:g.37821150_37821151del (hg19) chr17:g.39664897_39664898del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39664900_39664901del , CM000679.2:g.39664900_39664901del GRCh38
NC_000017.10:g.37821153_37821154del , CM000679.1:g.37821153_37821154del GRCh37
NC_000017.9:g.35074679_35074680del NCBI36
NG_008892.1:g.4555_4556del , LRG_210:g.4555_4556del
NG_042278.1:g.1920_1921del

Transcript Alleles

HGVS Amino-acid Change
ENST00000309889.2:c.-460_-459del ENSP00000312624.2:n.-460_-459del
Search 100 bp 5'
Search 100 bp 3'