Canonical Allele Identifier: CA1937420356

Gene: HABP2

Linked Data

• dbSNP Id: rs1845292659

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570793G>C , CM000672.2:g.113570793G>C	GRCh38
NC_000010.10:g.115330552G>C , CM000672.1:g.115330552G>C	GRCh37
NC_000010.9:g.115320542G>C	NCBI36
NG_008956.1:g.22775G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.106+3268G>C MANE Select	ENSP00000277903.4:n.106+3268G>C
ENST00000351270.3:c.106+3268G>C	ENSP00000277903.4:n.106+3268G>C
ENST00000542051.5:c.28+3268G>C	ENSP00000443283.1:n.28+3268G>C
NM_001177660.1:c.28+3268G>C	NP_001171131.1:n.28+3268G>C
NM_004132.3:c.106+3268G>C	NP_004123.1:n.106+3268G>C
NM_001177660.2:c.28+3268G>C	NP_001171131.1:n.28+3268G>C
NM_004132.4:c.106+3268G>C	NP_004123.1:n.106+3268G>C
NM_004132.5:c.106+3268G>C MANE Select	NP_004123.1:n.106+3268G>C
NM_001177660.3:c.28+3268G>C	NP_001171131.1:n.28+3268G>C