Canonical Allele Identifier: CA647210741
Gene: HNMT HGNC NCBI

Linked Data

gnomAD v4: 2-138001986-C-A
COSMIC: COSN21686934
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.138001986C>A , CM000664.2:g.138001986C>A GRCh38
NC_000002.11:g.138759556C>A , CM000664.1:g.138759556C>A GRCh37
NC_000002.10:g.138476026C>A NCBI36
NG_012966.1:g.42749C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000280097.5:c.299-78C>A MANE Select ENSP00000280097.3:n.299-78C>A
ENST00000280097.4:c.299-78C>A ENSP00000280097.3:n.299-78C>A
ENST00000410115.5:c.299-78C>A ENSP00000386940.1:n.299-78C>A
ENST00000467390.5:n.311-78C>A
ENST00000485653.1:n.231-78C>A
NM_006895.2:c.299-78C>A NP_008826.1:n.299-78C>A
XM_011511063.1:c.197-78C>A XP_011509365.1:n.197-78C>A
XM_011511064.1:c.-80-78C>A XP_011509366.1:n.-80-78C>A
XM_011511064.2:c.-80-78C>A XP_011509366.1:n.-80-78C>A
XM_017003948.1:c.197-78C>A XP_016859437.1:n.197-78C>A
XM_017003949.2:c.299-78C>A XP_016859438.1:n.299-78C>A
XR_001739719.1:n.1039+5003G>T
XR_002959286.1:n.686-78C>A
NM_006895.3:c.299-78C>A MANE Select NP_008826.1:n.299-78C>A
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