Canonical Allele Identifier: CA595756574

Gene: HABP2

Linked Data

• dbSNP Id: rs1187741907
• gnomAD v2: 10-115330690-G-C
• gnomAD v3: 10-113570931-G-C
• gnomAD v4: 10-113570931-G-C
• MyVariant Identifiers: chr10:g.115330690G>C (hg19) ; chr10:g.113570931G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.113570931G>C , CM000672.2:g.113570931G>C	GRCh38
NC_000010.10:g.115330690G>C , CM000672.1:g.115330690G>C	GRCh37
NC_000010.9:g.115320680G>C	NCBI36
NG_008956.1:g.22913G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000351270.4:c.107-3358G>C MANE Select	ENSP00000277903.4:n.107-3358G>C
ENST00000351270.3:c.107-3358G>C	ENSP00000277903.4:n.107-3358G>C
ENST00000542051.5:c.29-3358G>C	ENSP00000443283.1:n.29-3358G>C
NM_001177660.1:c.29-3358G>C	NP_001171131.1:n.29-3358G>C
NM_004132.3:c.107-3358G>C	NP_004123.1:n.107-3358G>C
NM_001177660.2:c.29-3358G>C	NP_001171131.1:n.29-3358G>C
NM_004132.4:c.107-3358G>C	NP_004123.1:n.107-3358G>C
NM_004132.5:c.107-3358G>C MANE Select	NP_004123.1:n.107-3358G>C
NM_001177660.3:c.29-3358G>C	NP_001171131.1:n.29-3358G>C