Canonical Allele Identifier: CA563603844
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs1309250879

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100845A>G , CM000667.2:g.151100845A>G GRCh38
NC_000005.9:g.150480406A>G , CM000667.1:g.150480406A>G GRCh37
NC_000005.8:g.150460599A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*603T>C MANE Select ENSP00000346550.5:n.*603T>C
ENST00000522664.5:c.318T>C
NM_001155.4:c.*603T>C NP_001146.2:n.*603T>C
NM_001193544.1:c.*603T>C NP_001180473.1:n.*603T>C
NM_001363114.1:c.*603T>C NP_001350043.1:n.*603T>C
NM_001155.5:c.*603T>C MANE Select NP_001146.2:n.*603T>C
NM_001193544.2:c.*603T>C NP_001180473.1:n.*603T>C
NM_001363114.2:c.*603T>C NP_001350043.1:n.*603T>C