Canonical Allele Identifier: CA417703405
Gene: MMACHC HGNC NCBI

Linked Data

gnomAD v4: 1-45500341-G-T
MyVariant Identifiers: chr1:g.45966013G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500341G>T , CM000663.2:g.45500341G>T GRCh38
NC_000001.10:g.45966013G>T , CM000663.1:g.45966013G>T GRCh37
NC_000001.9:g.45738600G>T NCBI36
NG_013378.1:g.5158G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000401061.9:c.9G>T MANE Select ENSP00000383840.4:p.Pro3=
ENST00000401061.8:c.9G>T ENSP00000383840.4:p.Pro3=
ENST00000616135.1:c.-163G>T ENSP00000478859.1:n.-163G>T
NM_015506.2:c.9G>T NP_056321.2:p.Pro3=
XM_005270724.3:c.9G>T XP_005270781.1:p.Pro3=
XM_011541204.1:c.-214G>T XP_011539506.1:n.-214G>T
NM_001330540.1:c.-214G>T NP_001317469.1:n.-214G>T
XM_005270724.5:c.9G>T XP_005270781.1:p.Pro3=
NM_015506.3:c.9G>T MANE Select NP_056321.2:p.Pro3=
NM_001330540.2:c.-214G>T NP_001317469.1:n.-214G>T