Canonical Allele Identifier: CA151235469
Gene:

Linked Data

dbSNP Id: rs374625227
gnomAD v2: 6-161089736-ATGGTGT-A
gnomAD v3: 6-160668704-ATGGTGT-A
gnomAD v4: 6-160668704-ATGGTGT-A
MyVariant Identifiers: chr6:g.161089737_161089742del (hg19) chr6:g.160668705_160668710del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668710_160668715del , CM000668.2:g.160668710_160668715del GRCh38
NC_000006.11:g.161089742_161089747del , CM000668.1:g.161089742_161089747del GRCh37
NC_000006.10:g.161009732_161009737del NCBI36
NG_016147.1:g.2666_2671del

Transcript Alleles

HGVS Amino-acid change
ENST00000452651.1:n.115-2337_115-2332del
Search 100 bp 5'
Search 100 bp 3'