Canonical Allele Identifier: CA2655934852
Gene: MN1 HGNC NCBI

Linked Data

gnomAD v4: 22-27750912-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750912C>A , CM000684.2:g.27750912C>A GRCh38
NC_000022.10:g.28146900C>A , CM000684.1:g.28146900C>A GRCh37
NC_000022.9:g.26476900C>A NCBI36
NG_023258.1:g.55587G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.491G>T
ENST00000302326.5:c.*3G>T MANE Select ENSP00000304956.4:n.*3G>T
ENST00000302326.4:c.*3G>T ENSP00000304956.4:n.*3G>T
ENST00000424656.1:c.319G>T
ENST00000497225.1:n.322G>T
NM_002430.2:c.*3G>T NP_002421.3:n.*3G>T
NM_002430.3:c.*3G>T MANE Select NP_002421.3:n.*3G>T
Search 100 bp 5'
Search 100 bp 3'