Canonical Allele Identifier: CA551142760
Gene: GRXCR1 HGNC NCBI

Linked Data

dbSNP Id: rs1416586277
gnomAD v2: 4-42964840-T-C
gnomAD v3: 4-42962823-T-C
gnomAD v4: 4-42962823-T-C
MyVariant Identifiers: chr4:g.42964840T>C (hg19) chr4:g.42962823T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.42962823T>C , CM000666.2:g.42962823T>C GRCh38
NC_000004.11:g.42964840T>C , CM000666.1:g.42964840T>C GRCh37
NC_000004.10:g.42659597T>C NCBI36
NG_027718.1:g.74558T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000399770.3:c.385-69T>C MANE Select ENSP00000382670.2:n.385-69T>C
ENST00000399770.2:c.385-69T>C ENSP00000382670.2:n.385-69T>C
NM_001080476.2:c.385-69T>C NP_001073945.1:n.385-69T>C
XM_011513691.1:c.22-69T>C XP_011511993.1:n.22-69T>C
NM_001080476.3:c.385-69T>C MANE Select NP_001073945.1:n.385-69T>C
Search 100 bp 5'
Search 100 bp 3'