Canonical Allele Identifier: CA104731765

Gene: ANXA5

Linked Data

• dbSNP Id: rs549650618
• gnomAD v2: 4-122618072-G-C
• gnomAD v3: 4-121696917-G-C
• gnomAD v4: 4-121696917-G-C
• MyVariant Identifiers: chr4:g.122618072G>C (hg19) ; chr4:g.121696917G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.121696917G>C , CM000666.2:g.121696917G>C	GRCh38
NC_000004.11:g.122618072G>C , CM000666.1:g.122618072G>C	GRCh37
NC_000004.10:g.122837522G>C	NCBI36
NG_032042.1:g.5076C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296511.10:c.-90C>G MANE Select	ENSP00000296511.5:n.-90C>G
ENST00000296511.9:c.-90C>G	ENSP00000296511.5:n.-90C>G
ENST00000501272.6:c.-90C>G	ENSP00000424106.1:n.-90C>G
ENST00000506395.5:c.-90C>G	ENSP00000421421.1:n.-90C>G
ENST00000509016.5:n.76C>G
ENST00000511552.5:n.59C>G
ENST00000513428.5:n.76C>G
ENST00000513523.1:n.79C>G
ENST00000513728.1:c.-90C>G	ENSP00000427135.1:n.-90C>G
ENST00000515017.5:c.-90C>G	ENSP00000424199.1:n.-90C>G
NM_001154.3:c.-90C>G	NP_001145.1:n.-90C>G
XM_017008141.2:c.-90C>G	XP_016863630.1:n.-90C>G
NM_001154.4:c.-90C>G MANE Select	NP_001145.1:n.-90C>G