Canonical Allele Identifier: CA762354157

Gene: HIBCH

Linked Data

• dbSNP Id: rs1227381058
• gnomAD v3: 2-190248237-T-C
• gnomAD v4: 2-190248237-T-C
• MyVariant Identifiers: chr2:g.191112963T>C (hg19) ; chr2:g.190248237T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190248237T>C , CM000664.2:g.190248237T>C	GRCh38
NC_000002.11:g.191112963T>C , CM000664.1:g.191112963T>C	GRCh37
NC_000002.10:g.190821208T>C	NCBI36
NG_017062.1:g.76809A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000359678.10:c.750+1403A>G MANE Select	ENSP00000352706.5:n.750+1403A>G
ENST00000359678.9:c.750+1403A>G	ENSP00000352706.5:n.750+1403A>G
ENST00000392332.7:c.750+1403A>G	ENSP00000376144.3:n.750+1403A>G
ENST00000392333.7:c.367+1403A>G
ENST00000409820.2:c.90+1403A>G	ENSP00000387098.2:n.90+1403A>G
ENST00000410045.5:c.81+1403A>G	ENSP00000386274.1:n.81+1403A>G
ENST00000485992.1:n.371+1403A>G
ENST00000622246.4:c.732+1403A>G	ENSP00000481055.1:n.732+1403A>G
NM_014362.3:c.750+1403A>G	NP_055177.2:n.750+1403A>G
NM_198047.2:c.750+1403A>G	NP_932164.1:n.750+1403A>G
XM_011510953.1:c.750+1403A>G	XP_011509255.1:n.750+1403A>G
XM_011510954.1:c.252+1403A>G	XP_011509256.1:n.252+1403A>G
XR_922903.1:n.994+1403A>G
XM_011510953.2:c.750+1403A>G	XP_011509255.1:n.750+1403A>G
XR_922903.2:n.813+1403A>G
NM_014362.4:c.750+1403A>G MANE Select	NP_055177.2:n.750+1403A>G
NM_198047.3:c.750+1403A>G	NP_932164.1:n.750+1403A>G