Canonical Allele Identifier: CA417703465

Gene: MMACHC

Linked Data

• MyVariant Identifiers: chr1:g.45966061T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45500389T>C , CM000663.2:g.45500389T>C	GRCh38
NC_000001.10:g.45966061T>C , CM000663.1:g.45966061T>C	GRCh37
NC_000001.9:g.45738648T>C	NCBI36
NG_013378.1:g.5206T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.57T>C MANE Select	ENSP00000383840.4:p.Phe19=
ENST00000401061.8:c.57T>C	ENSP00000383840.4:p.Phe19=
ENST00000616135.1:c.-115T>C	ENSP00000478859.1:n.-115T>C
NM_015506.2:c.57T>C	NP_056321.2:p.Phe19=
XM_005270724.3:c.57T>C	XP_005270781.1:p.Phe19=
XM_011541204.1:c.-166T>C	XP_011539506.1:n.-166T>C
NM_001330540.1:c.-166T>C	NP_001317469.1:n.-166T>C
XM_005270724.5:c.57T>C	XP_005270781.1:p.Phe19=
NM_015506.3:c.57T>C MANE Select	NP_056321.2:p.Phe19=
NM_001330540.2:c.-166T>C	NP_001317469.1:n.-166T>C