Canonical Allele Identifier: CA405301685
Gene: HAMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.35775920A>C (hg19) chr19:g.35285017A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.35285017A>C , CM000681.2:g.35285017A>C GRCh38
NC_000019.9:g.35775920A>C , CM000681.1:g.35775920A>C GRCh37
NC_000019.8:g.40467760A>C NCBI36
NG_011563.1:g.7511A>C
NG_011563.2:g.7511A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000222304.5:c.230A>C MANE Select ENSP00000222304.2:p.Lys77Thr
ENST00000222304.3:c.230A>C ENSP00000222304.2:p.Lys77Thr
ENST00000593580.1:n.2501A>C
ENST00000598398.5:c.230A>C ENSP00000471894.1:p.Lys77Thr
NM_021175.2:c.230A>C NP_066998.1:p.Lys77Thr
NM_021175.3:c.230A>C NP_066998.1:p.Lys77Thr
NM_021175.4:c.230A>C MANE Select NP_066998.1:p.Lys77Thr
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