Canonical Allele Identifier: CA405300584
Gene: HAMP HGNC NCBI

Linked Data

dbSNP Id: rs1200392968
gnomAD v2: 19-35775711-T-C
gnomAD v4: 19-35284808-T-C
MyVariant Identifiers: chr19:g.35775711T>C (hg19) chr19:g.35284808T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35284808T>C , CM000681.2:g.35284808T>C GRCh38
NC_000019.9:g.35775711T>C , CM000681.1:g.35775711T>C GRCh37
NC_000019.8:g.40467551T>C NCBI36
NG_011563.1:g.7302T>C
NG_011563.2:g.7302T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000222304.5:c.110T>C MANE Select ENSP00000222304.2:p.Leu37Pro
ENST00000222304.3:c.110T>C ENSP00000222304.2:p.Leu37Pro
ENST00000593580.1:n.2292T>C
ENST00000598398.5:c.110T>C ENSP00000471894.1:p.Leu37Pro
NM_021175.2:c.110T>C NP_066998.1:p.Leu37Pro
NM_021175.3:c.110T>C NP_066998.1:p.Leu37Pro
NM_021175.4:c.110T>C MANE Select NP_066998.1:p.Leu37Pro
Search 100 bp 5'
Search 100 bp 3'