Canonical Allele Identifier: CA349894340
Community Standard Title: NM_014362.4(HIBCH):c.941T>A (p.Leu314His)
Gene: HIBCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190213026A>T , CM000664.2:g.190213026A>T GRCh38
NC_000002.11:g.191077752A>T , CM000664.1:g.191077752A>T GRCh37
NC_000002.10:g.190785997A>T NCBI36
NG_017062.1:g.112020T>A

Transcript Alleles

HGVS Amino-acid Change
NM_014362.4:c.941T>A MANE Select NP_055177.2:p.Leu314His
ENST00000359678.10:c.941T>A MANE Select ENSP00000352706.5:p.Leu314His
NM_014362.3:c.941T>A NP_055177.2:p.Leu314His
NM_198047.2:c.941T>A NP_932164.1:p.Leu314His
NM_198047.3:c.941T>A NP_932164.1:p.Leu314His
ENST00000359678.9:c.941T>A ENSP00000352706.5:p.Leu314His
ENST00000392332.7:c.941T>A ENSP00000376144.3:p.Leu314His
ENST00000409820.2:c.281T>A ENSP00000387098.2:p.Leu94His
ENST00000410045.5:c.272T>A ENSP00000386274.1:p.Leu91His
ENST00000416732.5:c.194T>A ENSP00000399263.1:p.Leu65His
ENST00000486981.1:n.210T>A
ENST00000489147.1:n.3084T>A
ENST00000622246.4:c.923T>A ENSP00000481055.1:p.Leu308His
XM_011510953.1:c.941T>A XP_011509255.1:p.Leu314His
XM_011510953.2:c.941T>A XP_011509255.1:p.Leu314His
XM_011510954.1:c.443T>A XP_011509256.1:p.Leu148His
XR_922903.1:n.1185T>A
XR_922903.2:n.1004T>A