Canonical Allele Identifier: CA290433659

Gene: TCAP

Linked Data

• dbSNP Id: rs77831798
• gnomAD v3: 17-39665348-T-G
• gnomAD v4: 17-39665348-T-G
• MyVariant Identifiers: chr17:g.37821601T>G (hg19) ; chr17:g.39665348T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665348T>G , CM000679.2:g.39665348T>G	GRCh38
NC_000017.10:g.37821601T>G , CM000679.1:g.37821601T>G	GRCh37
NC_000017.9:g.35075127T>G	NCBI36
NG_008892.1:g.5003T>G , LRG_210:g.5003T>G
NG_042278.1:g.2368T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-12T>G	ENSP00000312624.2:n.-12T>G
NM_003673.3:c.-12T>G , LRG_210t1:c.-12T>G	NP_003664.1:n.-12T>G