Canonical Allele Identifier: CA349894333
Community Standard Title: NM_014362.4(HIBCH):c.944T>G (p.Met315Arg)
Gene: HIBCH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.190213023A>C , CM000664.2:g.190213023A>C GRCh38
NC_000002.11:g.191077749A>C , CM000664.1:g.191077749A>C GRCh37
NC_000002.10:g.190785994A>C NCBI36
NG_017062.1:g.112023T>G

Transcript Alleles

HGVS Amino-acid Change
NM_014362.4:c.944T>G MANE Select NP_055177.2:p.Met315Arg
ENST00000359678.10:c.944T>G MANE Select ENSP00000352706.5:p.Met315Arg
NM_014362.3:c.944T>G NP_055177.2:p.Met315Arg
NM_198047.2:c.944T>G NP_932164.1:p.Met315Arg
NM_198047.3:c.944T>G NP_932164.1:p.Met315Arg
ENST00000359678.9:c.944T>G ENSP00000352706.5:p.Met315Arg
ENST00000392332.7:c.944T>G ENSP00000376144.3:p.Met315Arg
ENST00000409820.2:c.284T>G ENSP00000387098.2:p.Met95Arg
ENST00000410045.5:c.275T>G ENSP00000386274.1:p.Met92Arg
ENST00000416732.5:c.197T>G ENSP00000399263.1:p.Met66Arg
ENST00000486981.1:n.213T>G
ENST00000489147.1:n.3087T>G
ENST00000622246.4:c.926T>G ENSP00000481055.1:p.Met309Arg
XM_011510953.1:c.944T>G XP_011509255.1:p.Met315Arg
XM_011510953.2:c.944T>G XP_011509255.1:p.Met315Arg
XM_011510954.1:c.446T>G XP_011509256.1:p.Met149Arg
XR_922903.1:n.1188T>G
XR_922903.2:n.1007T>G