Canonical Allele Identifier: CA214431713

Gene: HABP2

Linked Data

• dbSNP Id: rs745604355
• MyVariant Identifiers: chr10:g.115330816T>C (hg19) ; chr10:g.113571057T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113571057T>C , CM000672.2:g.113571057T>C	GRCh38
NC_000010.10:g.115330816T>C , CM000672.1:g.115330816T>C	GRCh37
NC_000010.9:g.115320806T>C	NCBI36
NG_008956.1:g.23039T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351270.4:c.107-3232T>C MANE Select	ENSP00000277903.4:n.107-3232T>C
ENST00000351270.3:c.107-3232T>C	ENSP00000277903.4:n.107-3232T>C
ENST00000542051.5:c.29-3232T>C	ENSP00000443283.1:n.29-3232T>C
NM_001177660.1:c.29-3232T>C	NP_001171131.1:n.29-3232T>C
NM_004132.3:c.107-3232T>C	NP_004123.1:n.107-3232T>C
NM_001177660.2:c.29-3232T>C	NP_001171131.1:n.29-3232T>C
NM_004132.4:c.107-3232T>C	NP_004123.1:n.107-3232T>C
NM_004132.5:c.107-3232T>C MANE Select	NP_004123.1:n.107-3232T>C
NM_001177660.3:c.29-3232T>C	NP_001171131.1:n.29-3232T>C