Canonical Allele Identifier: CA214431602

Gene: HABP2

Linked Data

• dbSNP Id: rs1029888381
• gnomAD v3: 10-113570824-A-T
• gnomAD v4: 10-113570824-A-T
• MyVariant Identifiers: chr10:g.115330583A>T (hg19) ; chr10:g.113570824A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570824A>T , CM000672.2:g.113570824A>T	GRCh38
NC_000010.10:g.115330583A>T , CM000672.1:g.115330583A>T	GRCh37
NC_000010.9:g.115320573A>T	NCBI36
NG_008956.1:g.22806A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.106+3299A>T MANE Select	ENSP00000277903.4:n.106+3299A>T
ENST00000351270.3:c.106+3299A>T	ENSP00000277903.4:n.106+3299A>T
ENST00000542051.5:c.28+3299A>T	ENSP00000443283.1:n.28+3299A>T
NM_001177660.1:c.28+3299A>T	NP_001171131.1:n.28+3299A>T
NM_004132.3:c.106+3299A>T	NP_004123.1:n.106+3299A>T
NM_001177660.2:c.28+3299A>T	NP_001171131.1:n.28+3299A>T
NM_004132.4:c.106+3299A>T	NP_004123.1:n.106+3299A>T
NM_004132.5:c.106+3299A>T MANE Select	NP_004123.1:n.106+3299A>T
NM_001177660.3:c.28+3299A>T	NP_001171131.1:n.28+3299A>T