Canonical Allele Identifier: CA1937429335
Gene: HABP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.113588565C= , CM000672.2:g.113588565C= GRCh38
NC_000010.10:g.115348324C= , CM000672.1:g.115348324C= GRCh37
NC_000010.9:g.115338314C= NCBI36
NG_008956.1:g.40547C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000351270.4:c.*196C= MANE Select ENSP00000277903.4:n.*196C=
ENST00000351270.3:c.*196C= ENSP00000277903.4:n.*196C=
ENST00000542051.5:c.*196C= ENSP00000443283.1:n.*196C=
NM_001177660.1:c.*196C= NP_001171131.1:n.*196C=
NM_004132.3:c.*196C= NP_004123.1:n.*196C=
NM_001177660.2:c.*196C= NP_001171131.1:n.*196C=
NM_004132.4:c.*196C= NP_004123.1:n.*196C=
NM_004132.5:c.*196C= MANE Select NP_004123.1:n.*196C=
NM_001177660.3:c.*196C= NP_001171131.1:n.*196C=
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