Canonical Allele Identifier: CA349894355
Community Standard Title: NM_014362.4(HIBCH):c.934A>G (p.Arg312Gly)
Gene: HIBCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190213033T>C , CM000664.2:g.190213033T>C GRCh38
NC_000002.11:g.191077759T>C , CM000664.1:g.191077759T>C GRCh37
NC_000002.10:g.190786004T>C NCBI36
NG_017062.1:g.112013A>G

Transcript Alleles

HGVS Amino-acid Change
NM_014362.4:c.934A>G MANE Select NP_055177.2:p.Arg312Gly
ENST00000359678.10:c.934A>G MANE Select ENSP00000352706.5:p.Arg312Gly
NM_014362.3:c.934A>G NP_055177.2:p.Arg312Gly
NM_198047.2:c.934A>G NP_932164.1:p.Arg312Gly
NM_198047.3:c.934A>G NP_932164.1:p.Arg312Gly
ENST00000359678.9:c.934A>G ENSP00000352706.5:p.Arg312Gly
ENST00000392332.7:c.934A>G ENSP00000376144.3:p.Arg312Gly
ENST00000409820.2:c.274A>G ENSP00000387098.2:p.Arg92Gly
ENST00000410045.5:c.265A>G ENSP00000386274.1:p.Arg89Gly
ENST00000416732.5:c.187A>G ENSP00000399263.1:p.Arg63Gly
ENST00000486981.1:n.203A>G
ENST00000489147.1:n.3077A>G
ENST00000622246.4:c.916A>G ENSP00000481055.1:p.Arg306Gly
XM_011510953.1:c.934A>G XP_011509255.1:p.Arg312Gly
XM_011510953.2:c.934A>G XP_011509255.1:p.Arg312Gly
XM_011510954.1:c.436A>G XP_011509256.1:p.Arg146Gly
XR_922903.1:n.1178A>G
XR_922903.2:n.997A>G