Canonical Allele Identifier: CA552292716

Gene: GC

Linked Data

• dbSNP Id: rs1382198365
• gnomAD v2: 4-72650472-AAGTT-A
• gnomAD v3: 4-71784755-AAGTT-A
• gnomAD v4: 4-71784755-AAGTT-A
• MyVariant Identifiers: chr4:g.72650473_72650476del (hg19) ; chr4:g.71784756_71784759del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784759_71784762del , CM000666.2:g.71784759_71784762del	GRCh38
NC_000004.11:g.72650476_72650479del , CM000666.1:g.72650476_72650479del	GRCh37
NC_000004.10:g.72869340_72869343del	NCBI36
NG_012837.2:g.25762_25765del
NG_012837.3:g.25762_25765del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504199.5:c.22-705_22-702del	ENSP00000421725.1:n.22-705_22-702del
ENST00000506245.1:c.-36-705_-36-702del	ENSP00000426718.1:n.-36-705_-36-702del
NM_001204306.1:c.-36-705_-36-702del	NP_001191235.1:n.-36-705_-36-702del
NM_001204307.1:c.22-705_22-702del	NP_001191236.1:n.22-705_22-702del