Canonical Allele Identifier: CA836921614
Gene:

Linked Data

dbSNP Id: rs1401177558
MyVariant Identifiers: chr7:g.24322278del (hg19) chr7:g.24282659del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.24282661del , CM000669.2:g.24282661del GRCh38
NC_000007.13:g.24322280del , CM000669.1:g.24322280del GRCh37
NC_000007.12:g.24288805del NCBI36
NG_016148.1:g.3474del

Transcript Alleles

HGVS Amino-acid change
XM_017012910.1:c.42-26960del XP_016868399.1:n.42-26960del
XM_017012911.1:c.42-26960del XP_016868400.1:n.42-26960del
XR_001745121.1:n.473+36698del
XR_001745122.1:n.345-85630del
XR_001745123.1:n.473+36698del
XR_001745124.1:n.473+36698del
XR_001745125.1:n.473+36698del
XR_001745126.1:n.473+36698del
XR_001745127.1:n.345-26960del
XR_001745129.1:n.473+36698del
XR_001745130.1:n.473+36698del
XR_001745131.1:n.473+36698del
XR_001745132.1:n.473+36698del
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