Canonical Allele Identifier: CA827778

Gene: MMACHC

Linked Data

• dbSNP Id: rs761889099
• ExAC: 1:45974561 C / T
• gnomAD v2: 1-45974561-C-T
• gnomAD v4: 1-45508889-C-T
• MyVariant Identifiers: chr1:g.45974561C>T (hg19) ; chr1:g.45508889C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508889C>T , CM000663.2:g.45508889C>T	GRCh38
NC_000001.10:g.45974561C>T , CM000663.1:g.45974561C>T	GRCh37
NC_000001.9:g.45747148C>T	NCBI36
NG_013378.1:g.13706C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000401061.9:c.523C>T MANE Select	ENSP00000383840.4:p.Pro175Ser
ENST00000401061.8:c.523C>T	ENSP00000383840.4:p.Pro175Ser
ENST00000616135.1:c.352C>T	ENSP00000478859.1:p.Pro118Ser
NM_015506.2:c.523C>T	NP_056321.2:p.Pro175Ser
XM_005270724.3:c.328C>T	XP_005270781.1:p.Pro110Ser
XM_011541204.1:c.352C>T	XP_011539506.1:p.Pro118Ser
NM_001330540.1:c.352C>T	NP_001317469.1:p.Pro118Ser
XM_005270724.5:c.328C>T	XP_005270781.1:p.Pro110Ser
NM_015506.3:c.523C>T MANE Select	NP_056321.2:p.Pro175Ser
NM_001330540.2:c.352C>T	NP_001317469.1:p.Pro118Ser