Canonical Allele Identifier: CA625938586

Gene: TCAP

Linked Data

• dbSNP Id: rs1418973988
• gnomAD v2: 17-37821109-GCA-G
• gnomAD v3: 17-39664856-GCA-G
• gnomAD v4: 17-39664856-GCA-G
• MyVariant Identifiers: chr17:g.37821110_37821111del (hg19) ; chr17:g.39664857_39664858del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39664858_39664859del , CM000679.2:g.39664858_39664859del	GRCh38
NC_000017.10:g.37821111_37821112del , CM000679.1:g.37821111_37821112del	GRCh37
NC_000017.9:g.35074637_35074638del	NCBI36
NG_008892.1:g.4513_4514del , LRG_210:g.4513_4514del
NG_042278.1:g.1878_1879del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-502_-501del	ENSP00000312624.2:n.-502_-501del