Canonical Allele Identifier: CA3516484
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs60849314
ExAC: 5:150480569 T / G
gnomAD v2: 5-150480569-T-G
gnomAD v3: 5-151101008-T-G
gnomAD v4: 5-151101008-T-G
MyVariant Identifiers: chr5:g.150480569T>G (hg19) chr5:g.151101008T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151101008T>G , CM000667.2:g.151101008T>G GRCh38
NC_000005.9:g.150480569T>G , CM000667.1:g.150480569T>G GRCh37
NC_000005.8:g.150460762T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*440A>C MANE Select ENSP00000346550.5:n.*440A>C
ENST00000522664.5:c.201-46A>C
NM_001155.4:c.*440A>C NP_001146.2:n.*440A>C
NM_001193544.1:c.*440A>C NP_001180473.1:n.*440A>C
NM_001363114.1:c.*440A>C NP_001350043.1:n.*440A>C
NM_001155.5:c.*440A>C MANE Select NP_001146.2:n.*440A>C
NM_001193544.2:c.*440A>C NP_001180473.1:n.*440A>C
NM_001363114.2:c.*440A>C NP_001350043.1:n.*440A>C
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