Canonical Allele Identifier: CA536178991
Gene: HNMT HGNC NCBI

Linked Data

dbSNP Id: rs1211104223

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.138002005A>G , CM000664.2:g.138002005A>G GRCh38
NC_000002.11:g.138759575A>G , CM000664.1:g.138759575A>G GRCh37
NC_000002.10:g.138476045A>G NCBI36
NG_012966.1:g.42768A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000280097.5:c.299-59A>G MANE Select ENSP00000280097.3:n.299-59A>G
ENST00000280097.4:c.299-59A>G ENSP00000280097.3:n.299-59A>G
ENST00000410115.5:c.299-59A>G ENSP00000386940.1:n.299-59A>G
ENST00000467390.5:n.311-59A>G
ENST00000485653.1:n.231-59A>G
NM_006895.2:c.299-59A>G NP_008826.1:n.299-59A>G
XM_011511063.1:c.197-59A>G XP_011509365.1:n.197-59A>G
XM_011511064.1:c.-80-59A>G XP_011509366.1:n.-80-59A>G
XM_011511064.2:c.-80-59A>G XP_011509366.1:n.-80-59A>G
XM_017003948.1:c.197-59A>G XP_016859437.1:n.197-59A>G
XM_017003949.2:c.299-59A>G XP_016859438.1:n.299-59A>G
XR_001739719.1:n.1039+4984T>C
XR_002959286.1:n.686-59A>G
NM_006895.3:c.299-59A>G MANE Select NP_008826.1:n.299-59A>G