Canonical Allele Identifier: CA329957411
Gene: AMER1 HGNC NCBI

Linked Data

dbSNP Id: rs1002861566

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.64192399T>C , CM000685.2:g.64192399T>C GRCh38
NC_000023.10:g.63412279T>C , CM000685.1:g.63412279T>C GRCh37
NC_000023.9:g.63329004T>C NCBI36
NG_021345.1:g.18346A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000374869.8:c.888A>G MANE Select ENSP00000364003.4:p.Gly296=
ENST00000330258.3:c.888A>G ENSP00000329117.3:p.Gly296=
ENST00000374869.7:c.888A>G ENSP00000364003.3:p.Gly296=
NM_152424.3:c.888A>G NP_689637.3:p.Gly296=
XM_011530858.1:c.888A>G XP_011529160.1:p.Gly296=
NM_152424.4:c.888A>G MANE Select NP_689637.3:p.Gly296=