Canonical Allele Identifier: CA701182645

Gene: LINC00331

Linked Data

• dbSNP Id: rs1455247523
• gnomAD v3: 13-78836360-GCA-G
• gnomAD v4: 13-78836360-GCA-G
• MyVariant Identifiers: chr13:g.79410496_79410497del (hg19) ; chr13:g.78836361_78836362del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.78836372_78836373del , CM000675.2:g.78836372_78836373del	GRCh38
NC_000013.10:g.79410507_79410508del , CM000675.1:g.79410507_79410508del	GRCh37
NC_000013.9:g.78308508_78308509del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_046869.2:n.111+3578_111+3579del