Canonical Allele Identifier: CA735235355

Gene:

Linked Data

• dbSNP Id: rs1466989388
• gnomAD v3: 1-34523656-CTA-C
• gnomAD v4: 1-34523656-CTA-C
• MyVariant Identifiers: chr1:g.34989258_34989259del (hg19) ; chr1:g.34523657_34523658del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.34523658_34523659del , CM000663.2:g.34523658_34523659del	GRCh38
NC_000001.10:g.34989259_34989260del , CM000663.1:g.34989259_34989260del	GRCh37
NC_000001.9:g.34761846_34761847del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
XR_947171.1:n.1073+23921_1073+23922del
XR_001737964.1:n.991+23921_991+23922del