Canonical Allele Identifier: CA99696469

Gene: ALB

Linked Data

• dbSNP Id: rs867930468
• gnomAD v2: 4-74270114-C-T
• gnomAD v4: 4-73404397-C-T
• MyVariant Identifiers: chr4:g.74270114C>T (hg19) ; chr4:g.73404397C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404397C>T , CM000666.2:g.73404397C>T	GRCh38
NC_000004.11:g.74270114C>T , CM000666.1:g.74270114C>T	GRCh37
NC_000004.10:g.74488978C>T	NCBI36
NG_009291.1:g.5143C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.70C>T MANE Select	ENSP00000295897.4:p.Arg24Ter
ENST00000295897.8:c.70C>T	ENSP00000295897.4:p.Arg24Ter
ENST00000401494.7:c.70C>T	ENSP00000384695.3:p.Arg24Ter
ENST00000415165.6:c.70C>T	ENSP00000401820.2:p.Arg24Ter
ENST00000441319.5:c.76C>T	ENSP00000392541.1:p.Arg26Ter
ENST00000476441.6:c.70C>T	ENSP00000423727.1:p.Arg24Ter
ENST00000503124.5:c.-111C>T	ENSP00000421027.1:n.-111C>T
ENST00000509063.5:c.70C>T	ENSP00000422784.1:p.Arg24Ter
ENST00000510166.5:n.111C>T
ENST00000514786.1:n.48+61C>T
ENST00000515133.5:n.111C>T
ENST00000621085.4:c.70C>T	ENSP00000483421.1:p.Arg24Ter
ENST00000621628.4:c.70C>T	ENSP00000480485.1:p.Arg24Ter
NM_000477.5:c.70C>T	NP_000468.1:p.Arg24Ter
NM_000477.6:c.70C>T	NP_000468.1:p.Arg24Ter
NM_000477.7:c.70C>T MANE Select	NP_000468.1:p.Arg24Ter