Canonical Allele Identifier: CA214431553
Gene: HABP2 HGNC NCBI

Linked Data

dbSNP Id: rs760523657
gnomAD v2: 10-115330490-A-AT
gnomAD v3: 10-113570731-A-AT
gnomAD v4: 10-113570731-A-AT
MyVariant Identifiers: chr10:g.115330490_115330491insT (hg19) chr10:g.113570731_113570732insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570738dup , CM000672.2:g.113570738dup GRCh38
NC_000010.10:g.115330497dup , CM000672.1:g.115330497dup GRCh37
NC_000010.9:g.115320487dup NCBI36
NG_008956.1:g.22720dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.106+3213dup MANE Select ENSP00000277903.4:n.106+3213dup
ENST00000351270.3:c.106+3213dup ENSP00000277903.4:n.106+3213dup
ENST00000542051.5:c.28+3213dup ENSP00000443283.1:n.28+3213dup
NM_001177660.1:c.28+3213dup NP_001171131.1:n.28+3213dup
NM_004132.3:c.106+3213dup NP_004123.1:n.106+3213dup
NM_001177660.2:c.28+3213dup NP_001171131.1:n.28+3213dup
NM_004132.4:c.106+3213dup NP_004123.1:n.106+3213dup
NM_004132.5:c.106+3213dup MANE Select NP_004123.1:n.106+3213dup
NM_001177660.3:c.28+3213dup NP_001171131.1:n.28+3213dup
Search 100 bp 5'
Search 100 bp 3'