Canonical Allele Identifier: CA3516479
Gene: ANXA6 HGNC NCBI

Linked Data

dbSNP Id: rs776494079
ExAC: 5:150480421 C / A
gnomAD v2: 5-150480421-C-A
gnomAD v4: 5-151100860-C-A
MyVariant Identifiers: chr5:g.150480421C>A (hg19) chr5:g.151100860C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.151100860C>A , CM000667.2:g.151100860C>A GRCh38
NC_000005.9:g.150480421C>A , CM000667.1:g.150480421C>A GRCh37
NC_000005.8:g.150460614C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000354546.10:c.*588G>T MANE Select ENSP00000346550.5:n.*588G>T
ENST00000522664.5:c.303G>T
NM_001155.4:c.*588G>T NP_001146.2:n.*588G>T
NM_001193544.1:c.*588G>T NP_001180473.1:n.*588G>T
NM_001363114.1:c.*588G>T NP_001350043.1:n.*588G>T
NM_001155.5:c.*588G>T MANE Select NP_001146.2:n.*588G>T
NM_001193544.2:c.*588G>T NP_001180473.1:n.*588G>T
NM_001363114.2:c.*588G>T NP_001350043.1:n.*588G>T
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