Canonical Allele Identifier: CA1594212918
Gene: ADAM19 HGNC NCBI

Linked Data

dbSNP Id: rs1756148857
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.157518186C>T , CM000667.2:g.157518186C>T GRCh38
NC_000005.9:g.156945194C>T , CM000667.1:g.156945194C>T GRCh37
NC_000005.8:g.156877772C>T NCBI36
NG_046960.1:g.62638G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000257527.9:c.666+637G>A MANE Select ENSP00000257527.5:n.666+637G>A
ENST00000257527.8:c.666+637G>A ENSP00000257527.4:n.666+637G>A
ENST00000517905.1:c.666+637G>A ENSP00000428654.1:n.666+637G>A
ENST00000517951.5:c.666+637G>A ENSP00000428376.1:n.666+637G>A
NM_033274.4:c.666+637G>A NP_150377.1:n.666+637G>A
XM_005266003.2:c.666+637G>A XP_005266060.1:n.666+637G>A
XM_011534680.1:c.-135-4681G>A XP_011532982.1:n.-135-4681G>A
XM_011534681.1:c.-145-4681G>A XP_011532983.1:n.-145-4681G>A
NM_033274.5:c.666+637G>A MANE Select NP_150377.1:n.666+637G>A
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