Canonical Allele Identifier: CA1937429366
Gene: HABP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588624T= , CM000672.2:g.113588624T= GRCh38
NC_000010.10:g.115348383T= , CM000672.1:g.115348383T= GRCh37
NC_000010.9:g.115338373T= NCBI36
NG_008956.1:g.40606T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*255T= MANE Select ENSP00000277903.4:n.*255T=
ENST00000351270.3:c.*255T= ENSP00000277903.4:n.*255T=
ENST00000542051.5:c.*255T= ENSP00000443283.1:n.*255T=
NM_001177660.1:c.*255T= NP_001171131.1:n.*255T=
NM_004132.3:c.*255T= NP_004123.1:n.*255T=
NM_001177660.2:c.*255T= NP_001171131.1:n.*255T=
NM_004132.4:c.*255T= NP_004123.1:n.*255T=
NM_004132.5:c.*255T= MANE Select NP_004123.1:n.*255T=
NM_001177660.3:c.*255T= NP_001171131.1:n.*255T=