Canonical Allele Identifier: CA21825861
Gene: MMACHC HGNC NCBI

Linked Data

dbSNP Id: rs903704063
gnomAD v3: 1-45500256-G-C
gnomAD v4: 1-45500256-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.45500256G>C , CM000663.2:g.45500256G>C GRCh38
NC_000001.10:g.45965928G>C , CM000663.1:g.45965928G>C GRCh37
NC_000001.9:g.45738515G>C NCBI36
NG_013378.1:g.5073G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000401061.8:c.-77G>C ENSP00000383840.4:n.-77G>C
NM_015506.2:c.-77G>C NP_056321.2:n.-77G>C
NM_001330540.1:c.-299G>C NP_001317469.1:n.-299G>C
XM_005270724.5:c.-77G>C XP_005270781.1:n.-77G>C