Canonical Allele Identifier: CA413008122

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43950028T>C , CM000685.2:g.43950028T>C GRCh38
NC_000023.10:g.43809274T>C , CM000685.1:g.43809274T>C GRCh37
NC_000023.9:g.43694218T>C NCBI36
NG_009832.1:g.28648A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.175-2A>G (NDP) MANE Select ENSP00000495972.1:n.175-2A>G
ENST00000647044.1:c.175-2A>G (NDP) ENSP00000495811.1:n.175-2A>G
ENST00000378062.5:c.175-2A>G (NDP) ENSP00000367301.5:n.175-2A>G
ENST00000470584.1:n.219-2A>G (NDP)
NM_000266.3:c.175-2A>G (NDP) NP_000257.1:n.175-2A>G
NR_046631.1:n.297T>C (NDP-AS1)
NM_000266.4:c.175-2A>G (NDP) MANE Select NP_000257.1:n.175-2A>G