Canonical Allele Identifier: CA1937420366
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113570819A= , CM000672.2:g.113570819A= GRCh38
NC_000010.10:g.115330578A= , CM000672.1:g.115330578A= GRCh37
NC_000010.9:g.115320568A= NCBI36
NG_008956.1:g.22801A=

Transcript Alleles

HGVS Amino-acid change
ENST00000351270.4:c.106+3294A= MANE Select ENSP00000277903.4:n.106+3294A=
ENST00000351270.3:c.106+3294A= ENSP00000277903.4:n.106+3294A=
ENST00000542051.5:c.28+3294A= ENSP00000443283.1:n.28+3294A=
NM_001177660.1:c.28+3294A= NP_001171131.1:n.28+3294A=
NM_004132.3:c.106+3294A= NP_004123.1:n.106+3294A=
NM_001177660.2:c.28+3294A= NP_001171131.1:n.28+3294A=
NM_004132.4:c.106+3294A= NP_004123.1:n.106+3294A=
NM_004132.5:c.106+3294A= MANE Select NP_004123.1:n.106+3294A=
NM_001177660.3:c.28+3294A= NP_001171131.1:n.28+3294A=