Canonical Allele Identifier: CA151235360
Gene:

Linked Data

dbSNP Id: rs377558433
gnomAD v2: 6-161089578-G-GGGCA
gnomAD v3: 6-160668546-G-GGGCA
gnomAD v4: 6-160668546-G-GGGCA
MyVariant Identifiers: chr6:g.161089578_161089579insGGCA (hg19) chr6:g.160668546_160668547insGGCA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.160668548_160668551dup , CM000668.2:g.160668548_160668551dup GRCh38
NC_000006.11:g.161089580_161089583dup , CM000668.1:g.161089580_161089583dup GRCh37
NC_000006.10:g.161009570_161009573dup NCBI36
NG_016147.1:g.2826_2829dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000452651.1:n.115-2177_115-2174dup
Search 100 bp 5'
Search 100 bp 3'