Canonical Allele Identifier: CA155828791

Gene:

Linked Data

• dbSNP Id: rs3037354
• gnomAD v2: 7-24322925-CTG-C
• gnomAD v3: 7-24283306-CTG-C
• gnomAD v4: 7-24283306-CTG-C
• MyVariant Identifiers: chr7:g.24322926_24322927del (hg19) ; chr7:g.24283307_24283308del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.24283308_24283309del , CM000669.2:g.24283308_24283309del	GRCh38
NC_000007.13:g.24322927_24322928del , CM000669.1:g.24322927_24322928del	GRCh37
NC_000007.12:g.24289452_24289453del	NCBI36
NG_016148.1:g.4121_4122del

Transcript Alleles

HGVS	Amino-acid Change
XM_017012910.1:c.42-27609_42-27608del	XP_016868399.1:n.42-27609_42-27608del
XM_017012911.1:c.42-27609_42-27608del	XP_016868400.1:n.42-27609_42-27608del
XR_001745121.1:n.473+36049_473+36050del
XR_001745122.1:n.345-86279_345-86278del
XR_001745123.1:n.473+36049_473+36050del
XR_001745124.1:n.473+36049_473+36050del
XR_001745125.1:n.473+36049_473+36050del
XR_001745126.1:n.473+36049_473+36050del
XR_001745127.1:n.345-27609_345-27608del
XR_001745129.1:n.473+36049_473+36050del
XR_001745130.1:n.473+36049_473+36050del
XR_001745131.1:n.473+36049_473+36050del
XR_001745132.1:n.473+36049_473+36050del