Canonical Allele Identifier: CA736190766

Gene: MMACHC

Linked Data

• dbSNP Id: rs1326882577
• gnomAD v3: 1-45508526-T-C
• gnomAD v4: 1-45508526-T-C
• MyVariant Identifiers: chr1:g.45974198T>C (hg19) ; chr1:g.45508526T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.45508526T>C , CM000663.2:g.45508526T>C	GRCh38
NC_000001.10:g.45974198T>C , CM000663.1:g.45974198T>C	GRCh37
NC_000001.9:g.45746785T>C	NCBI36
NG_013378.1:g.13343T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000401061.9:c.429+162T>C MANE Select	ENSP00000383840.4:n.429+162T>C
ENST00000401061.8:c.429+162T>C	ENSP00000383840.4:n.429+162T>C
ENST00000616135.1:c.258+162T>C	ENSP00000478859.1:n.258+162T>C
NM_015506.2:c.429+162T>C	NP_056321.2:n.429+162T>C
XM_005270724.3:c.234+162T>C	XP_005270781.1:n.234+162T>C
XM_011541204.1:c.258+162T>C	XP_011539506.1:n.258+162T>C
NM_001330540.1:c.258+162T>C	NP_001317469.1:n.258+162T>C
XM_005270724.5:c.234+162T>C	XP_005270781.1:n.234+162T>C
NM_015506.3:c.429+162T>C MANE Select	NP_056321.2:n.429+162T>C
NM_001330540.2:c.258+162T>C	NP_001317469.1:n.258+162T>C