Canonical Allele Identifier: CA349893077

Gene: HIBCH

Linked Data

• MyVariant Identifiers: chr2:g.191069872A>T (hg19) ; chr2:g.190205146A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190205146A>T , CM000664.2:g.190205146A>T	GRCh38
NC_000002.11:g.191069872A>T , CM000664.1:g.191069872A>T	GRCh37
NC_000002.10:g.190778117A>T	NCBI36
NG_017062.1:g.119900T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359678.10:c.1132T>A MANE Select	ENSP00000352706.5:p.Ser378Thr
ENST00000359678.9:c.1132T>A	ENSP00000352706.5:p.Ser378Thr
ENST00000392332.7:c.*81T>A	ENSP00000376144.3:n.*81T>A
ENST00000399855.2:c.87T>A
ENST00000410045.5:c.463T>A	ENSP00000386274.1:p.Ser155Thr
ENST00000486981.1:n.367T>A
ENST00000622246.4:c.1114T>A	ENSP00000481055.1:p.Ser372Thr
NM_014362.3:c.1132T>A	NP_055177.2:p.Ser378Thr
NM_198047.2:c.*81T>A	NP_932164.1:n.*81T>A
XM_011510953.1:c.1132T>A	XP_011509255.1:p.Ser378Thr
XM_011510954.1:c.634T>A	XP_011509256.1:p.Ser212Thr
XR_922903.1:n.1342T>A
XM_011510953.2:c.1132T>A	XP_011509255.1:p.Ser378Thr
XR_922903.2:n.1161T>A
NM_014362.4:c.1132T>A MANE Select	NP_055177.2:p.Ser378Thr
NM_198047.3:c.*81T>A	NP_932164.1:n.*81T>A