Canonical Allele Identifier: CA21829165

Gene: MMACHC

Linked Data

• dbSNP Id: rs147660940
• MyVariant Identifiers: chr1:g.45973687T>G (hg19) ; chr1:g.45508015T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508015T>G , CM000663.2:g.45508015T>G	GRCh38
NC_000001.10:g.45973687T>G , CM000663.1:g.45973687T>G	GRCh37
NC_000001.9:g.45746274T>G	NCBI36
NG_013378.1:g.12832T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.277-197T>G MANE Select	ENSP00000383840.4:n.277-197T>G
ENST00000401061.8:c.277-197T>G	ENSP00000383840.4:n.277-197T>G
ENST00000616135.1:c.106-197T>G	ENSP00000478859.1:n.106-197T>G
NM_015506.2:c.277-197T>G	NP_056321.2:n.277-197T>G
XM_005270724.3:c.82-197T>G	XP_005270781.1:n.82-197T>G
XM_011541204.1:c.106-197T>G	XP_011539506.1:n.106-197T>G
NM_001330540.1:c.106-197T>G	NP_001317469.1:n.106-197T>G
XM_005270724.5:c.82-197T>G	XP_005270781.1:n.82-197T>G
NM_015506.3:c.277-197T>G MANE Select	NP_056321.2:n.277-197T>G
NM_001330540.2:c.106-197T>G	NP_001317469.1:n.106-197T>G