Canonical Allele Identifier: CA340131488

Gene: MMACHC

Linked Data

• dbSNP Id: rs1570829600
• MyVariant Identifiers: chr1:g.45973085A>C (hg19) ; chr1:g.45507413A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45507413A>C , CM000663.2:g.45507413A>C	GRCh38
NC_000001.10:g.45973085A>C , CM000663.1:g.45973085A>C	GRCh37
NC_000001.9:g.45745672A>C	NCBI36
NG_013378.1:g.12230A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.139A>C MANE Select	ENSP00000383840.4:p.Thr47Pro
ENST00000401061.8:c.139A>C	ENSP00000383840.4:p.Thr47Pro
ENST00000616135.1:c.-33A>C	ENSP00000478859.1:n.-33A>C
NM_015506.2:c.139A>C	NP_056321.2:p.Thr47Pro
XM_005270724.3:c.82-799A>C	XP_005270781.1:n.82-799A>C
XM_011541204.1:c.-33A>C	XP_011539506.1:n.-33A>C
NM_001330540.1:c.-33A>C	NP_001317469.1:n.-33A>C
XM_005270724.5:c.82-799A>C	XP_005270781.1:n.82-799A>C
NM_015506.3:c.139A>C MANE Select	NP_056321.2:p.Thr47Pro
NM_001330540.2:c.-33A>C	NP_001317469.1:n.-33A>C