Canonical Allele Identifier: CA2661302564
Gene: HNMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.138001987A>G , CM000664.2:g.138001987A>G GRCh38
NC_000002.11:g.138759557A>G , CM000664.1:g.138759557A>G GRCh37
NC_000002.10:g.138476027A>G NCBI36
NG_012966.1:g.42750A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000280097.5:c.299-77A>G MANE Select ENSP00000280097.3:n.299-77A>G
ENST00000280097.4:c.299-77A>G ENSP00000280097.3:n.299-77A>G
ENST00000410115.5:c.299-77A>G ENSP00000386940.1:n.299-77A>G
ENST00000467390.5:n.311-77A>G
ENST00000485653.1:n.231-77A>G
NM_006895.2:c.299-77A>G NP_008826.1:n.299-77A>G
XM_011511063.1:c.197-77A>G XP_011509365.1:n.197-77A>G
XM_011511064.1:c.-80-77A>G XP_011509366.1:n.-80-77A>G
XM_011511064.2:c.-80-77A>G XP_011509366.1:n.-80-77A>G
XM_017003948.1:c.197-77A>G XP_016859437.1:n.197-77A>G
XM_017003949.2:c.299-77A>G XP_016859438.1:n.299-77A>G
XR_001739719.1:n.1039+5002T>C
XR_002959286.1:n.686-77A>G
NM_006895.3:c.299-77A>G MANE Select NP_008826.1:n.299-77A>G