Canonical Allele Identifier: CA1922577297
Gene: MAT1A HGNC NCBI

Linked Data

dbSNP Id: rs1841444187
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.80273914G>A , CM000672.2:g.80273914G>A GRCh38
NC_000010.10:g.82033670G>A , CM000672.1:g.82033670G>A GRCh37
NC_000010.9:g.82023650G>A NCBI36
NG_008083.1:g.20765C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372213.8:c.1086-31C>T MANE Select ENSP00000361287.3:n.1086-31C>T
ENST00000372213.7:c.1086-31C>T ENSP00000361287.3:n.1086-31C>T
ENST00000480845.1:n.318-31C>T
ENST00000485270.5:n.598-31C>T
NM_000429.2:c.1086-31C>T NP_000420.1:n.1086-31C>T
XM_005269842.3:c.1086-31C>T XP_005269899.1:n.1086-31C>T
XM_005269843.3:c.963-31C>T XP_005269900.1:n.963-31C>T
NM_000429.3:c.1086-31C>T MANE Select NP_000420.1:n.1086-31C>T
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