Canonical Allele Identifier: CA1937420498

Gene: HABP2

Linked Data

• dbSNP Id: rs1845298903

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113571079T>C , CM000672.2:g.113571079T>C	GRCh38
NC_000010.10:g.115330838T>C , CM000672.1:g.115330838T>C	GRCh37
NC_000010.9:g.115320828T>C	NCBI36
NG_008956.1:g.23061T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.107-3210T>C MANE Select	ENSP00000277903.4:n.107-3210T>C
ENST00000351270.3:c.107-3210T>C	ENSP00000277903.4:n.107-3210T>C
ENST00000542051.5:c.29-3210T>C	ENSP00000443283.1:n.29-3210T>C
NM_001177660.1:c.29-3210T>C	NP_001171131.1:n.29-3210T>C
NM_004132.3:c.107-3210T>C	NP_004123.1:n.107-3210T>C
NM_001177660.2:c.29-3210T>C	NP_001171131.1:n.29-3210T>C
NM_004132.4:c.107-3210T>C	NP_004123.1:n.107-3210T>C
NM_004132.5:c.107-3210T>C MANE Select	NP_004123.1:n.107-3210T>C
NM_001177660.3:c.29-3210T>C	NP_001171131.1:n.29-3210T>C