Canonical Allele Identifier: CA625938782

Gene: TCAP

Linked Data

• dbSNP Id: rs1332399080
• gnomAD v2: 17-37821489-C-G
• gnomAD v3: 17-39665236-C-G
• gnomAD v4: 17-39665236-C-G
• MyVariant Identifiers: chr17:g.37821489C>G (hg19) ; chr17:g.39665236C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39665236C>G , CM000679.2:g.39665236C>G	GRCh38
NC_000017.10:g.37821489C>G , CM000679.1:g.37821489C>G	GRCh37
NC_000017.9:g.35075015C>G	NCBI36
NG_008892.1:g.4891C>G , LRG_210:g.4891C>G
NG_042278.1:g.2256C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.2:c.-124C>G	ENSP00000312624.2:n.-124C>G