Canonical Allele Identifier: CA21825919

Gene: MMACHC

Linked Data

• dbSNP Id: rs780981680
• MyVariant Identifiers: chr1:g.45966018T>C (hg19) ; chr1:g.45500346T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45500346T>C , CM000663.2:g.45500346T>C	GRCh38
NC_000001.10:g.45966018T>C , CM000663.1:g.45966018T>C	GRCh37
NC_000001.9:g.45738605T>C	NCBI36
NG_013378.1:g.5163T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000401061.9:c.14T>C MANE Select	ENSP00000383840.4:p.Val5Ala
ENST00000401061.8:c.14T>C	ENSP00000383840.4:p.Val5Ala
ENST00000616135.1:c.-158T>C	ENSP00000478859.1:n.-158T>C
NM_015506.2:c.14T>C	NP_056321.2:p.Val5Ala
XM_005270724.3:c.14T>C	XP_005270781.1:p.Val5Ala
XM_011541204.1:c.-209T>C	XP_011539506.1:n.-209T>C
NM_001330540.1:c.-209T>C	NP_001317469.1:n.-209T>C
XM_005270724.5:c.14T>C	XP_005270781.1:p.Val5Ala
NM_015506.3:c.14T>C MANE Select	NP_056321.2:p.Val5Ala
NM_001330540.2:c.-209T>C	NP_001317469.1:n.-209T>C