Canonical Allele Identifier: CA417703486

Gene: MMACHC

Linked Data

• MyVariant Identifiers: chr1:g.45966073T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45500401T>G , CM000663.2:g.45500401T>G	GRCh38
NC_000001.10:g.45966073T>G , CM000663.1:g.45966073T>G	GRCh37
NC_000001.9:g.45738660T>G	NCBI36
NG_013378.1:g.5218T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.69T>G MANE Select	ENSP00000383840.4:p.Val23=
ENST00000401061.8:c.69T>G	ENSP00000383840.4:p.Val23=
ENST00000616135.1:c.-103T>G	ENSP00000478859.1:n.-103T>G
NM_015506.2:c.69T>G	NP_056321.2:p.Val23=
XM_005270724.3:c.69T>G	XP_005270781.1:p.Val23=
XM_011541204.1:c.-154T>G	XP_011539506.1:n.-154T>G
NM_001330540.1:c.-154T>G	NP_001317469.1:n.-154T>G
XM_005270724.5:c.69T>G	XP_005270781.1:p.Val23=
NM_015506.3:c.69T>G MANE Select	NP_056321.2:p.Val23=
NM_001330540.2:c.-154T>G	NP_001317469.1:n.-154T>G