Canonical Allele Identifier: CA513939252
Gene: MN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.28146954C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.27750966C>G , CM000684.2:g.27750966C>G GRCh38
NC_000022.10:g.28146954C>G , CM000684.1:g.28146954C>G GRCh37
NC_000022.9:g.26476954C>G NCBI36
NG_023258.1:g.55533G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703102.1:n.437G>C
ENST00000302326.5:c.3912G>C MANE Select ENSP00000304956.4:p.Leu1304=
ENST00000302326.4:c.3912G>C ENSP00000304956.4:p.Leu1304=
ENST00000424656.1:c.265G>C
ENST00000497225.1:n.268G>C
NM_002430.2:c.3912G>C NP_002421.3:p.Leu1304=
NM_002430.3:c.3912G>C MANE Select NP_002421.3:p.Leu1304=