Canonical Allele Identifier: CA2261354384
Gene: GRN HGNC NCBI

Linked Data

dbSNP Id: rs2048378725
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44351891T>G , CM000679.2:g.44351891T>G GRCh38
NC_000017.10:g.42429259T>G , CM000679.1:g.42429259T>G GRCh37
NC_000017.9:g.39784785T>G NCBI36
NG_007886.1:g.11769T>G , LRG_661:g.11769T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000053867.8:c.1179+96T>G MANE Select ENSP00000053867.2:n.1179+96T>G
ENST00000639447.1:c.1136+139T>G ENSP00000492014.1:n.1136+139T>G
ENST00000053867.7:c.1179+96T>G ENSP00000053867.2:n.1179+96T>G
ENST00000586443.1:c.620+96T>G
ENST00000589265.5:c.708+96T>G ENSP00000467616.1:n.708+96T>G
NM_002087.3:c.1179+96T>G NP_002078.1:n.1179+96T>G
XM_005257253.1:c.1179+96T>G XP_005257310.1:n.1179+96T>G
XM_024450730.1:c.1179+96T>G XP_024306498.1:n.1179+96T>G
NM_002087.4:c.1179+96T>G MANE Select NP_002078.1:n.1179+96T>G
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