Canonical Allele Identifier: CA28646308

Gene: PSRC1

Linked Data

• dbSNP Id: rs534573875
• gnomAD v2: 1-109822177-A-C
• gnomAD v3: 1-109279555-A-C
• gnomAD v4: 1-109279555-A-C
• MyVariant Identifiers: chr1:g.109822177A>C (hg19) ; chr1:g.109279555A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109279555A>C , CM000663.2:g.109279555A>C	GRCh38
NC_000001.10:g.109822177A>C , CM000663.1:g.109822177A>C	GRCh37
NC_000001.9:g.109623700A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NM_001005290.3:c.*566T>G	NP_001005290.1:n.*566T>G
NM_001032291.2:c.*598T>G	NP_001027462.1:n.*598T>G
NM_032636.7:c.*598T>G	NP_116025.1:n.*598T>G
NM_001350237.1:c.*598T>G	NP_001337166.1:n.*598T>G
NM_001350238.1:c.*598T>G	NP_001337167.1:n.*598T>G
NM_001350239.1:c.*598T>G	NP_001337168.1:n.*598T>G
NM_001350240.1:c.*598T>G	NP_001337169.1:n.*598T>G
NM_001350241.1:c.*598T>G	NP_001337170.1:n.*598T>G
NM_001350242.1:c.*598T>G	NP_001337171.1:n.*598T>G
NM_001363309.1:c.*598T>G	NP_001350238.1:n.*598T>G