Canonical Allele Identifier: CA21829145

Gene: MMACHC

Linked Data

• dbSNP Id: rs938120670
• gnomAD v2: 1-45973675-C-T
• gnomAD v3: 1-45508003-C-T
• gnomAD v4: 1-45508003-C-T
• MyVariant Identifiers: chr1:g.45973675C>T (hg19) ; chr1:g.45508003C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508003C>T , CM000663.2:g.45508003C>T	GRCh38
NC_000001.10:g.45973675C>T , CM000663.1:g.45973675C>T	GRCh37
NC_000001.9:g.45746262C>T	NCBI36
NG_013378.1:g.12820C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.277-209C>T MANE Select	ENSP00000383840.4:n.277-209C>T
ENST00000401061.8:c.277-209C>T	ENSP00000383840.4:n.277-209C>T
ENST00000616135.1:c.106-209C>T	ENSP00000478859.1:n.106-209C>T
NM_015506.2:c.277-209C>T	NP_056321.2:n.277-209C>T
XM_005270724.3:c.82-209C>T	XP_005270781.1:n.82-209C>T
XM_011541204.1:c.106-209C>T	XP_011539506.1:n.106-209C>T
NM_001330540.1:c.106-209C>T	NP_001317469.1:n.106-209C>T
XM_005270724.5:c.82-209C>T	XP_005270781.1:n.82-209C>T
NM_015506.3:c.277-209C>T MANE Select	NP_056321.2:n.277-209C>T
NM_001330540.2:c.106-209C>T	NP_001317469.1:n.106-209C>T