Canonical Allele Identifier: CA1922577315
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs551820928
gnomAD v4: 10-80273924-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273924C>T , CM000672.2:g.80273924C>T GRCh38
NC_000010.10:g.82033680C>T , CM000672.1:g.82033680C>T GRCh37
NC_000010.9:g.82023660C>T NCBI36
NG_008083.1:g.20755G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1086-41G>A MANE Select ENSP00000361287.3:n.1086-41G>A
ENST00000372213.7:c.1086-41G>A ENSP00000361287.3:n.1086-41G>A
ENST00000480845.1:n.318-41G>A
ENST00000485270.5:n.598-41G>A
NM_000429.2:c.1086-41G>A NP_000420.1:n.1086-41G>A
XM_005269842.3:c.1086-41G>A XP_005269899.1:n.1086-41G>A
XM_005269843.3:c.963-41G>A XP_005269900.1:n.963-41G>A
NM_000429.3:c.1086-41G>A MANE Select NP_000420.1:n.1086-41G>A
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